Canonical Allele Identifier: CA1673311369
Gene: SYNE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152391585_152391595delinsAAAAAAAAAAG , CM000668.2:g.152391585_152391595delinsAAAAAAAAAAG GRCh38
NC_000006.11:g.152712720_152712730delinsAAAAAAAAAAG , CM000668.1:g.152712720_152712730delinsAAAAAAAAAAG GRCh37
NC_000006.10:g.152754413_152754423delinsAAAAAAAAAAG NCBI36
NG_012855.1:g.250805_250815delinsCTTTTTTTTTT
NG_012855.2:g.250805_250815delinsCTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367255.10:c.7713-27_7713-17delinsCTTTTTTTTTT MANE Select ENSP00000356224.5:n.7713-27_7713-17delinsCTTTTTTTTTT
ENST00000423061.6:c.7734-27_7734-17delinsCTTTTTTTTTT ENSP00000396024.1:n.7734-27_7734-17delinsCTTTTTTTTTT
ENST00000341594.9:c.7779-27_7779-17delinsCTTTTTTTTTT ENSP00000341887.6:n.7779-27_7779-17delinsCTTTTTTTTTT
ENST00000367255.9:c.7713-27_7713-17delinsCTTTTTTTTTT ENSP00000356224.5:n.7713-27_7713-17delinsCTTTTTTTTTT
ENST00000423061.5:c.7734-27_7734-17delinsCTTTTTTTTTT ENSP00000396024.1:n.7734-27_7734-17delinsCTTTTTTTTTT
ENST00000461872.6:n.7931-27_7931-17delinsCTTTTTTTTTT
NM_033071.3:c.7734-27_7734-17delinsCTTTTTTTTTT NP_149062.1:n.7734-27_7734-17delinsCTTTTTTTTTT
NM_182961.3:c.7713-27_7713-17delinsCTTTTTTTTTT NP_892006.3:n.7713-27_7713-17delinsCTTTTTTTTTT
XM_006715407.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715470.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715408.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715471.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715409.1:c.7713-27_7713-17delinsCTTTTTTTTTT XP_006715472.1:n.7713-27_7713-17delinsCTTTTTTTTTT
XM_006715410.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715473.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715411.1:c.7683-27_7683-17delinsCTTTTTTTTTT XP_006715474.1:n.7683-27_7683-17delinsCTTTTTTTTTT
XM_006715412.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715475.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715413.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715476.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715414.1:c.7662-27_7662-17delinsCTTTTTTTTTT XP_006715477.1:n.7662-27_7662-17delinsCTTTTTTTTTT
XM_006715415.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715478.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715416.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715479.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715417.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715480.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715420.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715483.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715421.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715484.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715422.1:c.7575-27_7575-17delinsCTTTTTTTTTT XP_006715485.1:n.7575-27_7575-17delinsCTTTTTTTTTT
XM_006715423.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715486.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715424.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715487.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715425.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715488.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_011535641.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_011533943.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_011535642.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_011533944.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_011535643.1:c.7569-27_7569-17delinsCTTTTTTTTTT XP_011533945.1:n.7569-27_7569-17delinsCTTTTTTTTTT
XM_011535644.1:c.6009-27_6009-17delinsCTTTTTTTTTT XP_011533946.1:n.6009-27_6009-17delinsCTTTTTTTTTT
XM_011535645.1:c.5502-27_5502-17delinsCTTTTTTTTTT XP_011533947.1:n.5502-27_5502-17delinsCTTTTTTTTTT
XM_011535646.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_011533948.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_011535647.1:c.969-27_969-17delinsCTTTTTTTTTT XP_011533949.1:n.969-27_969-17delinsCTTTTTTTTTT
XM_006715408.2:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715471.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715410.2:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715473.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715412.2:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715475.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715413.2:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715476.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715415.2:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715478.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715416.2:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715479.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715417.2:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715480.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715420.2:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715483.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715421.2:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715484.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715423.2:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715486.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715424.2:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715487.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_006715425.2:c.7734-27_7734-17delinsCTTTTTTTTTT XP_006715488.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_011535641.2:c.7734-27_7734-17delinsCTTTTTTTTTT XP_011533943.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_011535642.2:c.7734-27_7734-17delinsCTTTTTTTTTT XP_011533944.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_011535645.2:c.5502-27_5502-17delinsCTTTTTTTTTT XP_011533947.1:n.5502-27_5502-17delinsCTTTTTTTTTT
XM_017010608.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_016866097.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_017010609.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_016866098.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_017010610.1:c.7713-27_7713-17delinsCTTTTTTTTTT XP_016866099.1:n.7713-27_7713-17delinsCTTTTTTTTTT
XM_017010611.2:c.7707-27_7707-17delinsCTTTTTTTTTT XP_016866100.1:n.7707-27_7707-17delinsCTTTTTTTTTT
XM_017010612.1:c.7656-27_7656-17delinsCTTTTTTTTTT XP_016866101.1:n.7656-27_7656-17delinsCTTTTTTTTTT
XM_017010613.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_016866102.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_017010614.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_016866103.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_017010615.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_016866104.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_017010616.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_016866105.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_017010617.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_016866106.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_017010618.1:c.7734-27_7734-17delinsCTTTTTTTTTT XP_016866107.1:n.7734-27_7734-17delinsCTTTTTTTTTT
XM_017010619.1:c.6009-27_6009-17delinsCTTTTTTTTTT XP_016866108.1:n.6009-27_6009-17delinsCTTTTTTTTTT
XR_001743287.1:n.8217-27_8217-17delinsCTTTTTTTTTT
NM_182961.4:c.7713-27_7713-17delinsCTTTTTTTTTT MANE Select NP_892006.3:n.7713-27_7713-17delinsCTTTTTTTTTT
NM_033071.5:c.7734-27_7734-17delinsCTTTTTTTTTT NP_149062.2:n.7734-27_7734-17delinsCTTTTTTTTTT