Canonical Allele Identifier: CA452760832

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152690115A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152368980A>G , CM000668.2:g.152368980A>G	GRCh38
NC_000006.11:g.152690115A>G , CM000668.1:g.152690115A>G	GRCh37
NC_000006.10:g.152731808A>G	NCBI36
NG_012855.1:g.273420T>C
NG_012855.2:g.273420T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000454018.7:c.1150T>C	ENSP00000390858.4:p.Leu384=
ENST00000367255.10:c.9799T>C MANE Select	ENSP00000356224.5:p.Leu3267=
ENST00000423061.6:c.9820T>C	ENSP00000396024.1:p.Leu3274=
ENST00000341594.9:c.9865T>C	ENSP00000341887.6:p.Leu3289=
ENST00000367255.9:c.9799T>C	ENSP00000356224.5:p.Leu3267=
ENST00000423061.5:c.9820T>C	ENSP00000396024.1:p.Leu3274=
ENST00000454018.6:c.1147T>C	ENSP00000390858.3:p.Leu383=
ENST00000469439.1:c.244+491T>C
ENST00000471834.1:n.1348T>C
NM_033071.3:c.9820T>C	NP_149062.1:p.Leu3274=
NM_182961.3:c.9799T>C	NP_892006.3:p.Leu3267=
XM_006715407.1:c.9820T>C	XP_006715470.1:p.Leu3274=
XM_006715408.1:c.9820T>C	XP_006715471.1:p.Leu3274=
XM_006715409.1:c.9799T>C	XP_006715472.1:p.Leu3267=
XM_006715410.1:c.9820T>C	XP_006715473.1:p.Leu3274=
XM_006715411.1:c.9769T>C	XP_006715474.1:p.Leu3257=
XM_006715412.1:c.9820T>C	XP_006715475.1:p.Leu3274=
XM_006715413.1:c.9820T>C	XP_006715476.1:p.Leu3274=
XM_006715414.1:c.9748T>C	XP_006715477.1:p.Leu3250=
XM_006715415.1:c.9820T>C	XP_006715478.1:p.Leu3274=
XM_006715416.1:c.9820T>C	XP_006715479.1:p.Leu3274=
XM_006715417.1:c.9820T>C	XP_006715480.1:p.Leu3274=
XM_006715420.1:c.9820T>C	XP_006715483.1:p.Leu3274=
XM_006715421.1:c.9672+491T>C	XP_006715484.1:n.9672+491T>C
XM_006715422.1:c.9661T>C	XP_006715485.1:p.Leu3221=
XM_006715423.1:c.9820T>C	XP_006715486.1:p.Leu3274=
XM_006715424.1:c.9820T>C	XP_006715487.1:p.Leu3274=
XM_006715425.1:c.9820T>C	XP_006715488.1:p.Leu3274=
XM_011535641.1:c.9820T>C	XP_011533943.1:p.Leu3274=
XM_011535642.1:c.9820T>C	XP_011533944.1:p.Leu3274=
XM_011535643.1:c.9655T>C	XP_011533945.1:p.Leu3219=
XM_011535644.1:c.8095T>C	XP_011533946.1:p.Leu2699=
XM_011535645.1:c.7588T>C	XP_011533947.1:p.Leu2530=
XM_011535646.1:c.9820T>C	XP_011533948.1:p.Leu3274=
XM_011535647.1:c.3055T>C	XP_011533949.1:p.Leu1019=
XM_006715408.2:c.9820T>C	XP_006715471.1:p.Leu3274=
XM_006715410.2:c.9820T>C	XP_006715473.1:p.Leu3274=
XM_006715412.2:c.9820T>C	XP_006715475.1:p.Leu3274=
XM_006715413.2:c.9820T>C	XP_006715476.1:p.Leu3274=
XM_006715415.2:c.9820T>C	XP_006715478.1:p.Leu3274=
XM_006715416.2:c.9820T>C	XP_006715479.1:p.Leu3274=
XM_006715417.2:c.9820T>C	XP_006715480.1:p.Leu3274=
XM_006715420.2:c.9820T>C	XP_006715483.1:p.Leu3274=
XM_006715421.2:c.9672+491T>C	XP_006715484.1:n.9672+491T>C
XM_006715423.2:c.9820T>C	XP_006715486.1:p.Leu3274=
XM_006715424.2:c.9820T>C	XP_006715487.1:p.Leu3274=
XM_006715425.2:c.9820T>C	XP_006715488.1:p.Leu3274=
XM_011535641.2:c.9820T>C	XP_011533943.1:p.Leu3274=
XM_011535642.2:c.9820T>C	XP_011533944.1:p.Leu3274=
XM_011535645.2:c.7588T>C	XP_011533947.1:p.Leu2530=
XM_017010608.1:c.9820T>C	XP_016866097.1:p.Leu3274=
XM_017010609.1:c.9820T>C	XP_016866098.1:p.Leu3274=
XM_017010610.1:c.9799T>C	XP_016866099.1:p.Leu3267=
XM_017010611.2:c.9793T>C	XP_016866100.1:p.Leu3265=
XM_017010612.1:c.9742T>C	XP_016866101.1:p.Leu3248=
XM_017010613.1:c.9820T>C	XP_016866102.1:p.Leu3274=
XM_017010614.1:c.9820T>C	XP_016866103.1:p.Leu3274=
XM_017010615.1:c.9820T>C	XP_016866104.1:p.Leu3274=
XM_017010616.1:c.9820T>C	XP_016866105.1:p.Leu3274=
XM_017010617.1:c.9820T>C	XP_016866106.1:p.Leu3274=
XM_017010618.1:c.9820T>C	XP_016866107.1:p.Leu3274=
XM_017010619.1:c.8095T>C	XP_016866108.1:p.Leu2699=
XR_001743287.1:n.10303T>C
NM_182961.4:c.9799T>C MANE Select	NP_892006.3:p.Leu3267=
NM_033071.5:c.9820T>C	NP_149062.2:p.Leu3274=