Canonical Allele Identifier: CA366099160

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152534790G>C (hg19) ; chr6:g.152213655G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152213655G>C , CM000668.2:g.152213655G>C	GRCh38
NC_000006.11:g.152534790G>C , CM000668.1:g.152534790G>C	GRCh37
NC_000006.10:g.152576483G>C	NCBI36
NG_012855.1:g.428745C>G
NG_012855.2:g.428745C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.22451C>G MANE Select	ENSP00000356224.5:p.Ser7484Ter
ENST00000423061.6:c.22238C>G	ENSP00000396024.1:p.Ser7413Ter
ENST00000341594.9:c.21236C>G	ENSP00000341887.6:p.Ser7079Ter
ENST00000367251.7:c.1217C>G	ENSP00000356220.3:p.Ser406Ter
ENST00000367255.9:c.22451C>G	ENSP00000356224.5:p.Ser7484Ter
ENST00000367256.9:n.6143C>G
ENST00000367257.8:c.389C>G	ENSP00000356226.4:p.Ser130Ter
ENST00000409694.6:n.6035C>G
ENST00000423061.5:c.22238C>G	ENSP00000396024.1:p.Ser7413Ter
NM_033071.3:c.22238C>G	NP_149062.1:p.Ser7413Ter
NM_182961.3:c.22451C>G	NP_892006.3:p.Ser7484Ter
XM_006715407.1:c.22487C>G	XP_006715470.1:p.Ser7496Ter
XM_006715408.1:c.22475C>G	XP_006715471.1:p.Ser7492Ter
XM_006715409.1:c.22466C>G	XP_006715472.1:p.Ser7489Ter
XM_006715410.1:c.22487C>G	XP_006715473.1:p.Ser7496Ter
XM_006715411.1:c.22436C>G	XP_006715474.1:p.Ser7479Ter
XM_006715412.1:c.22472C>G	XP_006715475.1:p.Ser7491Ter
XM_006715413.1:c.22487C>G	XP_006715476.1:p.Ser7496Ter
XM_006715414.1:c.22415C>G	XP_006715477.1:p.Ser7472Ter
XM_006715415.1:c.22487C>G	XP_006715478.1:p.Ser7496Ter
XM_006715416.1:c.22472C>G	XP_006715479.1:p.Ser7491Ter
XM_006715417.1:c.22346C>G	XP_006715480.1:p.Ser7449Ter
XM_006715420.1:c.22334C>G	XP_006715483.1:p.Ser7445Ter
XM_006715421.1:c.22331C>G	XP_006715484.1:p.Ser7444Ter
XM_006715422.1:c.22328C>G	XP_006715485.1:p.Ser7443Ter
XM_006715423.1:c.22487C>G	XP_006715486.1:p.Ser7496Ter
XM_006715424.1:c.22487C>G	XP_006715487.1:p.Ser7496Ter
XM_006715425.1:c.22487C>G	XP_006715488.1:p.Ser7496Ter
XM_011535641.1:c.22484C>G	XP_011533943.1:p.Ser7495Ter
XM_011535642.1:c.22472C>G	XP_011533944.1:p.Ser7491Ter
XM_011535643.1:c.22322C>G	XP_011533945.1:p.Ser7441Ter
XM_011535644.1:c.20762C>G	XP_011533946.1:p.Ser6921Ter
XM_011535645.1:c.20255C>G	XP_011533947.1:p.Ser6752Ter
XM_011535647.1:c.15722C>G	XP_011533949.1:p.Ser5241Ter
XM_006715408.2:c.22475C>G	XP_006715471.1:p.Ser7492Ter
XM_006715410.2:c.22487C>G	XP_006715473.1:p.Ser7496Ter
XM_006715412.2:c.22472C>G	XP_006715475.1:p.Ser7491Ter
XM_006715413.2:c.22487C>G	XP_006715476.1:p.Ser7496Ter
XM_006715415.2:c.22487C>G	XP_006715478.1:p.Ser7496Ter
XM_006715416.2:c.22472C>G	XP_006715479.1:p.Ser7491Ter
XM_006715417.2:c.22346C>G	XP_006715480.1:p.Ser7449Ter
XM_006715420.2:c.22334C>G	XP_006715483.1:p.Ser7445Ter
XM_006715421.2:c.22331C>G	XP_006715484.1:p.Ser7444Ter
XM_006715423.2:c.22487C>G	XP_006715486.1:p.Ser7496Ter
XM_006715424.2:c.22487C>G	XP_006715487.1:p.Ser7496Ter
XM_006715425.2:c.22487C>G	XP_006715488.1:p.Ser7496Ter
XM_011535641.2:c.22484C>G	XP_011533943.1:p.Ser7495Ter
XM_011535642.2:c.22472C>G	XP_011533944.1:p.Ser7491Ter
XM_011535645.2:c.20255C>G	XP_011533947.1:p.Ser6752Ter
XM_017010608.1:c.22487C>G	XP_016866097.1:p.Ser7496Ter
XM_017010609.1:c.22487C>G	XP_016866098.1:p.Ser7496Ter
XM_017010610.1:c.22466C>G	XP_016866099.1:p.Ser7489Ter
XM_017010611.2:c.22460C>G	XP_016866100.1:p.Ser7487Ter
XM_017010612.1:c.22409C>G	XP_016866101.1:p.Ser7470Ter
XM_017010613.1:c.22484C>G	XP_016866102.1:p.Ser7495Ter
XM_017010614.1:c.22331C>G	XP_016866103.1:p.Ser7444Ter
XM_017010615.1:c.22331C>G	XP_016866104.1:p.Ser7444Ter
XM_017010616.1:c.22487C>G	XP_016866105.1:p.Ser7496Ter
XM_017010617.1:c.22484C>G	XP_016866106.1:p.Ser7495Ter
XM_017010618.1:c.22472C>G	XP_016866107.1:p.Ser7491Ter
XM_017010619.1:c.20762C>G	XP_016866108.1:p.Ser6921Ter
NM_182961.4:c.22451C>G MANE Select	NP_892006.3:p.Ser7484Ter
NM_033071.5:c.22238C>G	NP_149062.2:p.Ser7413Ter