Canonical Allele Identifier: CA2841504496

Gene: SYNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152323441del , CM000668.2:g.152323441del	GRCh38
NC_000006.11:g.152644576del , CM000668.1:g.152644576del	GRCh37
NC_000006.10:g.152686269del	NCBI36
NG_012855.1:g.318959del
NG_012855.2:g.318959del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.15917+37del MANE Select	ENSP00000356224.5:n.15917+37del
ENST00000423061.6:c.15704+37del	ENSP00000396024.1:n.15704+37del
ENST00000341594.9:c.14945+37del	ENSP00000341887.6:n.14945+37del
ENST00000367255.9:c.15917+37del	ENSP00000356224.5:n.15917+37del
ENST00000423061.5:c.15704+37del	ENSP00000396024.1:n.15704+37del
ENST00000448038.2:c.-2+37del	ENSP00000390975.2:n.-2+37del
ENST00000490135.6:n.3263+37del
NM_033071.3:c.15704+37del	NP_149062.1:n.15704+37del
NM_182961.3:c.15917+37del	NP_892006.3:n.15917+37del
XM_006715407.1:c.15938+37del	XP_006715470.1:n.15938+37del
XM_006715408.1:c.15938+37del	XP_006715471.1:n.15938+37del
XM_006715409.1:c.15917+37del	XP_006715472.1:n.15917+37del
XM_006715410.1:c.15938+37del	XP_006715473.1:n.15938+37del
XM_006715411.1:c.15887+37del	XP_006715474.1:n.15887+37del
XM_006715412.1:c.15938+37del	XP_006715475.1:n.15938+37del
XM_006715413.1:c.15938+37del	XP_006715476.1:n.15938+37del
XM_006715414.1:c.15866+37del	XP_006715477.1:n.15866+37del
XM_006715415.1:c.15938+37del	XP_006715478.1:n.15938+37del
XM_006715416.1:c.15938+37del	XP_006715479.1:n.15938+37del
XM_006715417.1:c.15938+37del	XP_006715480.1:n.15938+37del
XM_006715420.1:c.15938+37del	XP_006715483.1:n.15938+37del
XM_006715421.1:c.15782+37del	XP_006715484.1:n.15782+37del
XM_006715422.1:c.15779+37del	XP_006715485.1:n.15779+37del
XM_006715423.1:c.15938+37del	XP_006715486.1:n.15938+37del
XM_006715424.1:c.15938+37del	XP_006715487.1:n.15938+37del
XM_006715425.1:c.15938+37del	XP_006715488.1:n.15938+37del
XM_011535641.1:c.15938+37del	XP_011533943.1:n.15938+37del
XM_011535642.1:c.15938+37del	XP_011533944.1:n.15938+37del
XM_011535643.1:c.15773+37del	XP_011533945.1:n.15773+37del
XM_011535644.1:c.14213+37del	XP_011533946.1:n.14213+37del
XM_011535645.1:c.13706+37del	XP_011533947.1:n.13706+37del
XM_011535646.1:c.15938+37del	XP_011533948.1:n.15938+37del
XM_011535647.1:c.9173+37del	XP_011533949.1:n.9173+37del
XM_006715408.2:c.15938+37del	XP_006715471.1:n.15938+37del
XM_006715410.2:c.15938+37del	XP_006715473.1:n.15938+37del
XM_006715412.2:c.15938+37del	XP_006715475.1:n.15938+37del
XM_006715413.2:c.15938+37del	XP_006715476.1:n.15938+37del
XM_006715415.2:c.15938+37del	XP_006715478.1:n.15938+37del
XM_006715416.2:c.15938+37del	XP_006715479.1:n.15938+37del
XM_006715417.2:c.15938+37del	XP_006715480.1:n.15938+37del
XM_006715420.2:c.15938+37del	XP_006715483.1:n.15938+37del
XM_006715421.2:c.15782+37del	XP_006715484.1:n.15782+37del
XM_006715423.2:c.15938+37del	XP_006715486.1:n.15938+37del
XM_006715424.2:c.15938+37del	XP_006715487.1:n.15938+37del
XM_006715425.2:c.15938+37del	XP_006715488.1:n.15938+37del
XM_011535641.2:c.15938+37del	XP_011533943.1:n.15938+37del
XM_011535642.2:c.15938+37del	XP_011533944.1:n.15938+37del
XM_011535645.2:c.13706+37del	XP_011533947.1:n.13706+37del
XM_017010608.1:c.15938+37del	XP_016866097.1:n.15938+37del
XM_017010609.1:c.15938+37del	XP_016866098.1:n.15938+37del
XM_017010610.1:c.15917+37del	XP_016866099.1:n.15917+37del
XM_017010611.2:c.15911+37del	XP_016866100.1:n.15911+37del
XM_017010612.1:c.15860+37del	XP_016866101.1:n.15860+37del
XM_017010613.1:c.15938+37del	XP_016866102.1:n.15938+37del
XM_017010614.1:c.15938+37del	XP_016866103.1:n.15938+37del
XM_017010615.1:c.15938+37del	XP_016866104.1:n.15938+37del
XM_017010616.1:c.15938+37del	XP_016866105.1:n.15938+37del
XM_017010617.1:c.15938+37del	XP_016866106.1:n.15938+37del
XM_017010618.1:c.15938+37del	XP_016866107.1:n.15938+37del
XM_017010619.1:c.14213+37del	XP_016866108.1:n.14213+37del
XR_001743287.1:n.16421+37del
NM_182961.4:c.15917+37del MANE Select	NP_892006.3:n.15917+37del
NM_033071.5:c.15704+37del	NP_149062.2:n.15704+37del