Canonical Allele Identifier: CA1673300426

Gene: SYNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152369493C= , CM000668.2:g.152369493C=	GRCh38
NC_000006.11:g.152690628C= , CM000668.1:g.152690628C=	GRCh37
NC_000006.10:g.152732321C=	NCBI36
NG_012855.1:g.272907G=
NG_012855.2:g.272907G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454018.7:c.980G=	ENSP00000390858.4:p.Arg327=
ENST00000367255.10:c.9629G= MANE Select	ENSP00000356224.5:p.Arg3210=
ENST00000423061.6:c.9650G=	ENSP00000396024.1:p.Arg3217=
ENST00000341594.9:c.9695G=	ENSP00000341887.6:p.Arg3232=
ENST00000367255.9:c.9629G=	ENSP00000356224.5:p.Arg3210=
ENST00000423061.5:c.9650G=	ENSP00000396024.1:p.Arg3217=
ENST00000454018.6:c.977G=	ENSP00000390858.3:p.Arg326=
ENST00000469439.1:c.222G=
ENST00000471834.1:n.835G=
NM_033071.3:c.9650G=	NP_149062.1:p.Arg3217=
NM_182961.3:c.9629G=	NP_892006.3:p.Arg3210=
XM_006715407.1:c.9650G=	XP_006715470.1:p.Arg3217=
XM_006715408.1:c.9650G=	XP_006715471.1:p.Arg3217=
XM_006715409.1:c.9629G=	XP_006715472.1:p.Arg3210=
XM_006715410.1:c.9650G=	XP_006715473.1:p.Arg3217=
XM_006715411.1:c.9599G=	XP_006715474.1:p.Arg3200=
XM_006715412.1:c.9650G=	XP_006715475.1:p.Arg3217=
XM_006715413.1:c.9650G=	XP_006715476.1:p.Arg3217=
XM_006715414.1:c.9578G=	XP_006715477.1:p.Arg3193=
XM_006715415.1:c.9650G=	XP_006715478.1:p.Arg3217=
XM_006715416.1:c.9650G=	XP_006715479.1:p.Arg3217=
XM_006715417.1:c.9650G=	XP_006715480.1:p.Arg3217=
XM_006715420.1:c.9650G=	XP_006715483.1:p.Arg3217=
XM_006715421.1:c.9650G=	XP_006715484.1:p.Arg3217=
XM_006715422.1:c.9491G=	XP_006715485.1:p.Arg3164=
XM_006715423.1:c.9650G=	XP_006715486.1:p.Arg3217=
XM_006715424.1:c.9650G=	XP_006715487.1:p.Arg3217=
XM_006715425.1:c.9650G=	XP_006715488.1:p.Arg3217=
XM_011535641.1:c.9650G=	XP_011533943.1:p.Arg3217=
XM_011535642.1:c.9650G=	XP_011533944.1:p.Arg3217=
XM_011535643.1:c.9485G=	XP_011533945.1:p.Arg3162=
XM_011535644.1:c.7925G=	XP_011533946.1:p.Arg2642=
XM_011535645.1:c.7418G=	XP_011533947.1:p.Arg2473=
XM_011535646.1:c.9650G=	XP_011533948.1:p.Arg3217=
XM_011535647.1:c.2885G=	XP_011533949.1:p.Arg962=
XM_006715408.2:c.9650G=	XP_006715471.1:p.Arg3217=
XM_006715410.2:c.9650G=	XP_006715473.1:p.Arg3217=
XM_006715412.2:c.9650G=	XP_006715475.1:p.Arg3217=
XM_006715413.2:c.9650G=	XP_006715476.1:p.Arg3217=
XM_006715415.2:c.9650G=	XP_006715478.1:p.Arg3217=
XM_006715416.2:c.9650G=	XP_006715479.1:p.Arg3217=
XM_006715417.2:c.9650G=	XP_006715480.1:p.Arg3217=
XM_006715420.2:c.9650G=	XP_006715483.1:p.Arg3217=
XM_006715421.2:c.9650G=	XP_006715484.1:p.Arg3217=
XM_006715423.2:c.9650G=	XP_006715486.1:p.Arg3217=
XM_006715424.2:c.9650G=	XP_006715487.1:p.Arg3217=
XM_006715425.2:c.9650G=	XP_006715488.1:p.Arg3217=
XM_011535641.2:c.9650G=	XP_011533943.1:p.Arg3217=
XM_011535642.2:c.9650G=	XP_011533944.1:p.Arg3217=
XM_011535645.2:c.7418G=	XP_011533947.1:p.Arg2473=
XM_017010608.1:c.9650G=	XP_016866097.1:p.Arg3217=
XM_017010609.1:c.9650G=	XP_016866098.1:p.Arg3217=
XM_017010610.1:c.9629G=	XP_016866099.1:p.Arg3210=
XM_017010611.2:c.9623G=	XP_016866100.1:p.Arg3208=
XM_017010612.1:c.9572G=	XP_016866101.1:p.Arg3191=
XM_017010613.1:c.9650G=	XP_016866102.1:p.Arg3217=
XM_017010614.1:c.9650G=	XP_016866103.1:p.Arg3217=
XM_017010615.1:c.9650G=	XP_016866104.1:p.Arg3217=
XM_017010616.1:c.9650G=	XP_016866105.1:p.Arg3217=
XM_017010617.1:c.9650G=	XP_016866106.1:p.Arg3217=
XM_017010618.1:c.9650G=	XP_016866107.1:p.Arg3217=
XM_017010619.1:c.7925G=	XP_016866108.1:p.Arg2642=
XR_001743287.1:n.10133G=
NM_182961.4:c.9629G= MANE Select	NP_892006.3:p.Arg3210=
NM_033071.5:c.9650G=	NP_149062.2:p.Arg3217=