Canonical Allele Identifier: CA366138181

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152690622T>G (hg19) ; chr6:g.152369487T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152369487T>G , CM000668.2:g.152369487T>G	GRCh38
NC_000006.11:g.152690622T>G , CM000668.1:g.152690622T>G	GRCh37
NC_000006.10:g.152732315T>G	NCBI36
NG_012855.1:g.272913A>C
NG_012855.2:g.272913A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454018.7:c.986A>C	ENSP00000390858.4:p.Glu329Ala
ENST00000367255.10:c.9635A>C MANE Select	ENSP00000356224.5:p.Glu3212Ala
ENST00000423061.6:c.9656A>C	ENSP00000396024.1:p.Glu3219Ala
ENST00000341594.9:c.9701A>C	ENSP00000341887.6:p.Glu3234Ala
ENST00000367255.9:c.9635A>C	ENSP00000356224.5:p.Glu3212Ala
ENST00000423061.5:c.9656A>C	ENSP00000396024.1:p.Glu3219Ala
ENST00000454018.6:c.983A>C	ENSP00000390858.3:p.Glu328Ala
ENST00000469439.1:c.228A>C
ENST00000471834.1:n.841A>C
NM_033071.3:c.9656A>C	NP_149062.1:p.Glu3219Ala
NM_182961.3:c.9635A>C	NP_892006.3:p.Glu3212Ala
XM_006715407.1:c.9656A>C	XP_006715470.1:p.Glu3219Ala
XM_006715408.1:c.9656A>C	XP_006715471.1:p.Glu3219Ala
XM_006715409.1:c.9635A>C	XP_006715472.1:p.Glu3212Ala
XM_006715410.1:c.9656A>C	XP_006715473.1:p.Glu3219Ala
XM_006715411.1:c.9605A>C	XP_006715474.1:p.Glu3202Ala
XM_006715412.1:c.9656A>C	XP_006715475.1:p.Glu3219Ala
XM_006715413.1:c.9656A>C	XP_006715476.1:p.Glu3219Ala
XM_006715414.1:c.9584A>C	XP_006715477.1:p.Glu3195Ala
XM_006715415.1:c.9656A>C	XP_006715478.1:p.Glu3219Ala
XM_006715416.1:c.9656A>C	XP_006715479.1:p.Glu3219Ala
XM_006715417.1:c.9656A>C	XP_006715480.1:p.Glu3219Ala
XM_006715420.1:c.9656A>C	XP_006715483.1:p.Glu3219Ala
XM_006715421.1:c.9656A>C	XP_006715484.1:p.Glu3219Ala
XM_006715422.1:c.9497A>C	XP_006715485.1:p.Glu3166Ala
XM_006715423.1:c.9656A>C	XP_006715486.1:p.Glu3219Ala
XM_006715424.1:c.9656A>C	XP_006715487.1:p.Glu3219Ala
XM_006715425.1:c.9656A>C	XP_006715488.1:p.Glu3219Ala
XM_011535641.1:c.9656A>C	XP_011533943.1:p.Glu3219Ala
XM_011535642.1:c.9656A>C	XP_011533944.1:p.Glu3219Ala
XM_011535643.1:c.9491A>C	XP_011533945.1:p.Glu3164Ala
XM_011535644.1:c.7931A>C	XP_011533946.1:p.Glu2644Ala
XM_011535645.1:c.7424A>C	XP_011533947.1:p.Glu2475Ala
XM_011535646.1:c.9656A>C	XP_011533948.1:p.Glu3219Ala
XM_011535647.1:c.2891A>C	XP_011533949.1:p.Glu964Ala
XM_006715408.2:c.9656A>C	XP_006715471.1:p.Glu3219Ala
XM_006715410.2:c.9656A>C	XP_006715473.1:p.Glu3219Ala
XM_006715412.2:c.9656A>C	XP_006715475.1:p.Glu3219Ala
XM_006715413.2:c.9656A>C	XP_006715476.1:p.Glu3219Ala
XM_006715415.2:c.9656A>C	XP_006715478.1:p.Glu3219Ala
XM_006715416.2:c.9656A>C	XP_006715479.1:p.Glu3219Ala
XM_006715417.2:c.9656A>C	XP_006715480.1:p.Glu3219Ala
XM_006715420.2:c.9656A>C	XP_006715483.1:p.Glu3219Ala
XM_006715421.2:c.9656A>C	XP_006715484.1:p.Glu3219Ala
XM_006715423.2:c.9656A>C	XP_006715486.1:p.Glu3219Ala
XM_006715424.2:c.9656A>C	XP_006715487.1:p.Glu3219Ala
XM_006715425.2:c.9656A>C	XP_006715488.1:p.Glu3219Ala
XM_011535641.2:c.9656A>C	XP_011533943.1:p.Glu3219Ala
XM_011535642.2:c.9656A>C	XP_011533944.1:p.Glu3219Ala
XM_011535645.2:c.7424A>C	XP_011533947.1:p.Glu2475Ala
XM_017010608.1:c.9656A>C	XP_016866097.1:p.Glu3219Ala
XM_017010609.1:c.9656A>C	XP_016866098.1:p.Glu3219Ala
XM_017010610.1:c.9635A>C	XP_016866099.1:p.Glu3212Ala
XM_017010611.2:c.9629A>C	XP_016866100.1:p.Glu3210Ala
XM_017010612.1:c.9578A>C	XP_016866101.1:p.Glu3193Ala
XM_017010613.1:c.9656A>C	XP_016866102.1:p.Glu3219Ala
XM_017010614.1:c.9656A>C	XP_016866103.1:p.Glu3219Ala
XM_017010615.1:c.9656A>C	XP_016866104.1:p.Glu3219Ala
XM_017010616.1:c.9656A>C	XP_016866105.1:p.Glu3219Ala
XM_017010617.1:c.9656A>C	XP_016866106.1:p.Glu3219Ala
XM_017010618.1:c.9656A>C	XP_016866107.1:p.Glu3219Ala
XM_017010619.1:c.7931A>C	XP_016866108.1:p.Glu2644Ala
XR_001743287.1:n.10139A>C
NM_182961.4:c.9635A>C MANE Select	NP_892006.3:p.Glu3212Ala
NM_033071.5:c.9656A>C	NP_149062.2:p.Glu3219Ala