Canonical Allele Identifier: CA452748478

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152534846A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152213711A>G , CM000668.2:g.152213711A>G	GRCh38
NC_000006.11:g.152534846A>G , CM000668.1:g.152534846A>G	GRCh37
NC_000006.10:g.152576539A>G	NCBI36
NG_012855.1:g.428689T>C
NG_012855.2:g.428689T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.22395T>C MANE Select	ENSP00000356224.5:p.Cys7465=
ENST00000423061.6:c.22182T>C	ENSP00000396024.1:p.Cys7394=
ENST00000341594.9:c.21180T>C	ENSP00000341887.6:p.Cys7060=
ENST00000367251.7:c.1161T>C	ENSP00000356220.3:p.Cys387=
ENST00000367255.9:c.22395T>C	ENSP00000356224.5:p.Cys7465=
ENST00000367256.9:n.6087T>C
ENST00000367257.8:c.333T>C	ENSP00000356226.4:p.Cys111=
ENST00000409694.6:n.5979T>C
ENST00000423061.5:c.22182T>C	ENSP00000396024.1:p.Cys7394=
NM_033071.3:c.22182T>C	NP_149062.1:p.Cys7394=
NM_182961.3:c.22395T>C	NP_892006.3:p.Cys7465=
XM_006715407.1:c.22431T>C	XP_006715470.1:p.Cys7477=
XM_006715408.1:c.22419T>C	XP_006715471.1:p.Cys7473=
XM_006715409.1:c.22410T>C	XP_006715472.1:p.Cys7470=
XM_006715410.1:c.22431T>C	XP_006715473.1:p.Cys7477=
XM_006715411.1:c.22380T>C	XP_006715474.1:p.Cys7460=
XM_006715412.1:c.22416T>C	XP_006715475.1:p.Cys7472=
XM_006715413.1:c.22431T>C	XP_006715476.1:p.Cys7477=
XM_006715414.1:c.22359T>C	XP_006715477.1:p.Cys7453=
XM_006715415.1:c.22431T>C	XP_006715478.1:p.Cys7477=
XM_006715416.1:c.22416T>C	XP_006715479.1:p.Cys7472=
XM_006715417.1:c.22290T>C	XP_006715480.1:p.Cys7430=
XM_006715420.1:c.22278T>C	XP_006715483.1:p.Cys7426=
XM_006715421.1:c.22275T>C	XP_006715484.1:p.Cys7425=
XM_006715422.1:c.22272T>C	XP_006715485.1:p.Cys7424=
XM_006715423.1:c.22431T>C	XP_006715486.1:p.Cys7477=
XM_006715424.1:c.22431T>C	XP_006715487.1:p.Cys7477=
XM_006715425.1:c.22431T>C	XP_006715488.1:p.Cys7477=
XM_011535641.1:c.22428T>C	XP_011533943.1:p.Cys7476=
XM_011535642.1:c.22416T>C	XP_011533944.1:p.Cys7472=
XM_011535643.1:c.22266T>C	XP_011533945.1:p.Cys7422=
XM_011535644.1:c.20706T>C	XP_011533946.1:p.Cys6902=
XM_011535645.1:c.20199T>C	XP_011533947.1:p.Cys6733=
XM_011535647.1:c.15666T>C	XP_011533949.1:p.Cys5222=
XM_006715408.2:c.22419T>C	XP_006715471.1:p.Cys7473=
XM_006715410.2:c.22431T>C	XP_006715473.1:p.Cys7477=
XM_006715412.2:c.22416T>C	XP_006715475.1:p.Cys7472=
XM_006715413.2:c.22431T>C	XP_006715476.1:p.Cys7477=
XM_006715415.2:c.22431T>C	XP_006715478.1:p.Cys7477=
XM_006715416.2:c.22416T>C	XP_006715479.1:p.Cys7472=
XM_006715417.2:c.22290T>C	XP_006715480.1:p.Cys7430=
XM_006715420.2:c.22278T>C	XP_006715483.1:p.Cys7426=
XM_006715421.2:c.22275T>C	XP_006715484.1:p.Cys7425=
XM_006715423.2:c.22431T>C	XP_006715486.1:p.Cys7477=
XM_006715424.2:c.22431T>C	XP_006715487.1:p.Cys7477=
XM_006715425.2:c.22431T>C	XP_006715488.1:p.Cys7477=
XM_011535641.2:c.22428T>C	XP_011533943.1:p.Cys7476=
XM_011535642.2:c.22416T>C	XP_011533944.1:p.Cys7472=
XM_011535645.2:c.20199T>C	XP_011533947.1:p.Cys6733=
XM_017010608.1:c.22431T>C	XP_016866097.1:p.Cys7477=
XM_017010609.1:c.22431T>C	XP_016866098.1:p.Cys7477=
XM_017010610.1:c.22410T>C	XP_016866099.1:p.Cys7470=
XM_017010611.2:c.22404T>C	XP_016866100.1:p.Cys7468=
XM_017010612.1:c.22353T>C	XP_016866101.1:p.Cys7451=
XM_017010613.1:c.22428T>C	XP_016866102.1:p.Cys7476=
XM_017010614.1:c.22275T>C	XP_016866103.1:p.Cys7425=
XM_017010615.1:c.22275T>C	XP_016866104.1:p.Cys7425=
XM_017010616.1:c.22431T>C	XP_016866105.1:p.Cys7477=
XM_017010617.1:c.22428T>C	XP_016866106.1:p.Cys7476=
XM_017010618.1:c.22416T>C	XP_016866107.1:p.Cys7472=
XM_017010619.1:c.20706T>C	XP_016866108.1:p.Cys6902=
NM_182961.4:c.22395T>C MANE Select	NP_892006.3:p.Cys7465=
NM_033071.5:c.22182T>C	NP_149062.2:p.Cys7394=