Canonical Allele Identifier: CA150197335
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2436681
ClinVar RCV Id: RCV003139017
dbSNP Id: rs942721092

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152300649C>G , CM000668.2:g.152300649C>G GRCh38
NC_000006.11:g.152621784C>G , CM000668.1:g.152621784C>G GRCh37
NC_000006.10:g.152663477C>G NCBI36
NG_012855.1:g.341751G>C
NG_012855.2:g.341751G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367255.10:c.17674G>C MANE Select ENSP00000356224.5:p.Val5892Leu
ENST00000423061.6:c.17461G>C ENSP00000396024.1:p.Val5821Leu
ENST00000341594.9:c.16459G>C ENSP00000341887.6:p.Val5487Leu
ENST00000367255.9:c.17674G>C ENSP00000356224.5:p.Val5892Leu
ENST00000367256.9:n.1366G>C
ENST00000409694.6:n.1258G>C
ENST00000423061.5:c.17461G>C ENSP00000396024.1:p.Val5821Leu
ENST00000489156.1:n.401+1220G>C
ENST00000537033.1:c.340G>C ENSP00000443879.1:p.Val114Leu
ENST00000540663.5:c.207+1220G>C ENSP00000437411.1:n.207+1220G>C
NM_033071.3:c.17461G>C NP_149062.1:p.Val5821Leu
NM_182961.3:c.17674G>C NP_892006.3:p.Val5892Leu
XM_006715407.1:c.17695G>C XP_006715470.1:p.Val5899Leu
XM_006715408.1:c.17695G>C XP_006715471.1:p.Val5899Leu
XM_006715409.1:c.17674G>C XP_006715472.1:p.Val5892Leu
XM_006715410.1:c.17695G>C XP_006715473.1:p.Val5899Leu
XM_006715411.1:c.17644G>C XP_006715474.1:p.Val5882Leu
XM_006715412.1:c.17695G>C XP_006715475.1:p.Val5899Leu
XM_006715413.1:c.17695G>C XP_006715476.1:p.Val5899Leu
XM_006715414.1:c.17623G>C XP_006715477.1:p.Val5875Leu
XM_006715415.1:c.17695G>C XP_006715478.1:p.Val5899Leu
XM_006715416.1:c.17695G>C XP_006715479.1:p.Val5899Leu
XM_006715417.1:c.17562+1220G>C XP_006715480.1:n.17562+1220G>C
XM_006715420.1:c.17562+1220G>C XP_006715483.1:n.17562+1220G>C
XM_006715421.1:c.17539G>C XP_006715484.1:p.Val5847Leu
XM_006715422.1:c.17536G>C XP_006715485.1:p.Val5846Leu
XM_006715423.1:c.17695G>C XP_006715486.1:p.Val5899Leu
XM_006715424.1:c.17695G>C XP_006715487.1:p.Val5899Leu
XM_006715425.1:c.17695G>C XP_006715488.1:p.Val5899Leu
XM_011535641.1:c.17695G>C XP_011533943.1:p.Val5899Leu
XM_011535642.1:c.17695G>C XP_011533944.1:p.Val5899Leu
XM_011535643.1:c.17530G>C XP_011533945.1:p.Val5844Leu
XM_011535644.1:c.15970G>C XP_011533946.1:p.Val5324Leu
XM_011535645.1:c.15463G>C XP_011533947.1:p.Val5155Leu
XM_011535646.1:c.17695G>C XP_011533948.1:p.Val5899Leu
XM_011535647.1:c.10930G>C XP_011533949.1:p.Val3644Leu
XM_006715408.2:c.17695G>C XP_006715471.1:p.Val5899Leu
XM_006715410.2:c.17695G>C XP_006715473.1:p.Val5899Leu
XM_006715412.2:c.17695G>C XP_006715475.1:p.Val5899Leu
XM_006715413.2:c.17695G>C XP_006715476.1:p.Val5899Leu
XM_006715415.2:c.17695G>C XP_006715478.1:p.Val5899Leu
XM_006715416.2:c.17695G>C XP_006715479.1:p.Val5899Leu
XM_006715417.2:c.17562+1220G>C XP_006715480.1:n.17562+1220G>C
XM_006715420.2:c.17562+1220G>C XP_006715483.1:n.17562+1220G>C
XM_006715421.2:c.17539G>C XP_006715484.1:p.Val5847Leu
XM_006715423.2:c.17695G>C XP_006715486.1:p.Val5899Leu
XM_006715424.2:c.17695G>C XP_006715487.1:p.Val5899Leu
XM_006715425.2:c.17695G>C XP_006715488.1:p.Val5899Leu
XM_011535641.2:c.17695G>C XP_011533943.1:p.Val5899Leu
XM_011535642.2:c.17695G>C XP_011533944.1:p.Val5899Leu
XM_011535645.2:c.15463G>C XP_011533947.1:p.Val5155Leu
XM_017010608.1:c.17695G>C XP_016866097.1:p.Val5899Leu
XM_017010609.1:c.17695G>C XP_016866098.1:p.Val5899Leu
XM_017010610.1:c.17674G>C XP_016866099.1:p.Val5892Leu
XM_017010611.2:c.17668G>C XP_016866100.1:p.Val5890Leu
XM_017010612.1:c.17617G>C XP_016866101.1:p.Val5873Leu
XM_017010613.1:c.17695G>C XP_016866102.1:p.Val5899Leu
XM_017010614.1:c.17562+1220G>C XP_016866103.1:n.17562+1220G>C
XM_017010615.1:c.17562+1220G>C XP_016866104.1:n.17562+1220G>C
XM_017010616.1:c.17695G>C XP_016866105.1:p.Val5899Leu
XM_017010617.1:c.17695G>C XP_016866106.1:p.Val5899Leu
XM_017010618.1:c.17695G>C XP_016866107.1:p.Val5899Leu
XM_017010619.1:c.15970G>C XP_016866108.1:p.Val5324Leu
XR_001743287.1:n.18178G>C
NM_182961.4:c.17674G>C MANE Select NP_892006.3:p.Val5892Leu
NM_033071.5:c.17461G>C NP_149062.2:p.Val5821Leu