Canonical Allele Identifier: CA150206513
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 497337
dbSNP Id: rs373436725

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152310858A>G , CM000668.2:g.152310858A>G GRCh38
NC_000006.11:g.152631993A>G , CM000668.1:g.152631993A>G GRCh37
NC_000006.10:g.152673686A>G NCBI36
NG_012855.1:g.331542T>C
NG_012855.2:g.331542T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682252.1:n.797T>C
ENST00000684208.1:n.797T>C
ENST00000684643.1:n.886T>C
ENST00000367255.10:c.16726T>C MANE Select ENSP00000356224.5:p.Ser5576Pro
ENST00000423061.6:c.16513T>C ENSP00000396024.1:p.Ser5505Pro
ENST00000341594.9:c.15511T>C ENSP00000341887.6:p.Ser5171Pro
ENST00000367255.9:c.16726T>C ENSP00000356224.5:p.Ser5576Pro
ENST00000367256.9:n.418T>C
ENST00000409694.6:n.310T>C
ENST00000423061.5:c.16513T>C ENSP00000396024.1:p.Ser5505Pro
NM_033071.3:c.16513T>C NP_149062.1:p.Ser5505Pro
NM_182961.3:c.16726T>C NP_892006.3:p.Ser5576Pro
XM_006715407.1:c.16747T>C XP_006715470.1:p.Ser5583Pro
XM_006715408.1:c.16747T>C XP_006715471.1:p.Ser5583Pro
XM_006715409.1:c.16726T>C XP_006715472.1:p.Ser5576Pro
XM_006715410.1:c.16747T>C XP_006715473.1:p.Ser5583Pro
XM_006715411.1:c.16696T>C XP_006715474.1:p.Ser5566Pro
XM_006715412.1:c.16747T>C XP_006715475.1:p.Ser5583Pro
XM_006715413.1:c.16747T>C XP_006715476.1:p.Ser5583Pro
XM_006715414.1:c.16675T>C XP_006715477.1:p.Ser5559Pro
XM_006715415.1:c.16747T>C XP_006715478.1:p.Ser5583Pro
XM_006715416.1:c.16747T>C XP_006715479.1:p.Ser5583Pro
XM_006715417.1:c.16747T>C XP_006715480.1:p.Ser5583Pro
XM_006715420.1:c.16747T>C XP_006715483.1:p.Ser5583Pro
XM_006715421.1:c.16591T>C XP_006715484.1:p.Ser5531Pro
XM_006715422.1:c.16588T>C XP_006715485.1:p.Ser5530Pro
XM_006715423.1:c.16747T>C XP_006715486.1:p.Ser5583Pro
XM_006715424.1:c.16747T>C XP_006715487.1:p.Ser5583Pro
XM_006715425.1:c.16747T>C XP_006715488.1:p.Ser5583Pro
XM_011535641.1:c.16747T>C XP_011533943.1:p.Ser5583Pro
XM_011535642.1:c.16747T>C XP_011533944.1:p.Ser5583Pro
XM_011535643.1:c.16582T>C XP_011533945.1:p.Ser5528Pro
XM_011535644.1:c.15022T>C XP_011533946.1:p.Ser5008Pro
XM_011535645.1:c.14515T>C XP_011533947.1:p.Ser4839Pro
XM_011535646.1:c.16747T>C XP_011533948.1:p.Ser5583Pro
XM_011535647.1:c.9982T>C XP_011533949.1:p.Ser3328Pro
XM_006715408.2:c.16747T>C XP_006715471.1:p.Ser5583Pro
XM_006715410.2:c.16747T>C XP_006715473.1:p.Ser5583Pro
XM_006715412.2:c.16747T>C XP_006715475.1:p.Ser5583Pro
XM_006715413.2:c.16747T>C XP_006715476.1:p.Ser5583Pro
XM_006715415.2:c.16747T>C XP_006715478.1:p.Ser5583Pro
XM_006715416.2:c.16747T>C XP_006715479.1:p.Ser5583Pro
XM_006715417.2:c.16747T>C XP_006715480.1:p.Ser5583Pro
XM_006715420.2:c.16747T>C XP_006715483.1:p.Ser5583Pro
XM_006715421.2:c.16591T>C XP_006715484.1:p.Ser5531Pro
XM_006715423.2:c.16747T>C XP_006715486.1:p.Ser5583Pro
XM_006715424.2:c.16747T>C XP_006715487.1:p.Ser5583Pro
XM_006715425.2:c.16747T>C XP_006715488.1:p.Ser5583Pro
XM_011535641.2:c.16747T>C XP_011533943.1:p.Ser5583Pro
XM_011535642.2:c.16747T>C XP_011533944.1:p.Ser5583Pro
XM_011535645.2:c.14515T>C XP_011533947.1:p.Ser4839Pro
XM_017010608.1:c.16747T>C XP_016866097.1:p.Ser5583Pro
XM_017010609.1:c.16747T>C XP_016866098.1:p.Ser5583Pro
XM_017010610.1:c.16726T>C XP_016866099.1:p.Ser5576Pro
XM_017010611.2:c.16720T>C XP_016866100.1:p.Ser5574Pro
XM_017010612.1:c.16669T>C XP_016866101.1:p.Ser5557Pro
XM_017010613.1:c.16747T>C XP_016866102.1:p.Ser5583Pro
XM_017010614.1:c.16747T>C XP_016866103.1:p.Ser5583Pro
XM_017010615.1:c.16747T>C XP_016866104.1:p.Ser5583Pro
XM_017010616.1:c.16747T>C XP_016866105.1:p.Ser5583Pro
XM_017010617.1:c.16747T>C XP_016866106.1:p.Ser5583Pro
XM_017010618.1:c.16747T>C XP_016866107.1:p.Ser5583Pro
XM_017010619.1:c.15022T>C XP_016866108.1:p.Ser5008Pro
XR_001743287.1:n.17230T>C
NM_182961.4:c.16726T>C MANE Select NP_892006.3:p.Ser5576Pro
NM_033071.5:c.16513T>C NP_149062.2:p.Ser5505Pro