Canonical Allele Identifier: CA366099090

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152534776G>A (hg19) ; chr6:g.152213641G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152213641G>A , CM000668.2:g.152213641G>A	GRCh38
NC_000006.11:g.152534776G>A , CM000668.1:g.152534776G>A	GRCh37
NC_000006.10:g.152576469G>A	NCBI36
NG_012855.1:g.428759C>T
NG_012855.2:g.428759C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367255.10:c.22465C>T MANE Select	ENSP00000356224.5:p.His7489Tyr
ENST00000423061.6:c.22252C>T	ENSP00000396024.1:p.His7418Tyr
ENST00000341594.9:c.21250C>T	ENSP00000341887.6:p.His7084Tyr
ENST00000367251.7:c.1231C>T	ENSP00000356220.3:p.His411Tyr
ENST00000367255.9:c.22465C>T	ENSP00000356224.5:p.His7489Tyr
ENST00000367256.9:n.6157C>T
ENST00000367257.8:c.403C>T	ENSP00000356226.4:p.His135Tyr
ENST00000409694.6:n.6049C>T
ENST00000423061.5:c.22252C>T	ENSP00000396024.1:p.His7418Tyr
NM_033071.3:c.22252C>T	NP_149062.1:p.His7418Tyr
NM_182961.3:c.22465C>T	NP_892006.3:p.His7489Tyr
XM_006715407.1:c.22501C>T	XP_006715470.1:p.His7501Tyr
XM_006715408.1:c.22489C>T	XP_006715471.1:p.His7497Tyr
XM_006715409.1:c.22480C>T	XP_006715472.1:p.His7494Tyr
XM_006715410.1:c.22501C>T	XP_006715473.1:p.His7501Tyr
XM_006715411.1:c.22450C>T	XP_006715474.1:p.His7484Tyr
XM_006715412.1:c.22486C>T	XP_006715475.1:p.His7496Tyr
XM_006715413.1:c.22501C>T	XP_006715476.1:p.His7501Tyr
XM_006715414.1:c.22429C>T	XP_006715477.1:p.His7477Tyr
XM_006715415.1:c.22501C>T	XP_006715478.1:p.His7501Tyr
XM_006715416.1:c.22486C>T	XP_006715479.1:p.His7496Tyr
XM_006715417.1:c.22360C>T	XP_006715480.1:p.His7454Tyr
XM_006715420.1:c.22348C>T	XP_006715483.1:p.His7450Tyr
XM_006715421.1:c.22345C>T	XP_006715484.1:p.His7449Tyr
XM_006715422.1:c.22342C>T	XP_006715485.1:p.His7448Tyr
XM_006715423.1:c.22501C>T	XP_006715486.1:p.His7501Tyr
XM_006715424.1:c.22501C>T	XP_006715487.1:p.His7501Tyr
XM_006715425.1:c.22501C>T	XP_006715488.1:p.His7501Tyr
XM_011535641.1:c.22498C>T	XP_011533943.1:p.His7500Tyr
XM_011535642.1:c.22486C>T	XP_011533944.1:p.His7496Tyr
XM_011535643.1:c.22336C>T	XP_011533945.1:p.His7446Tyr
XM_011535644.1:c.20776C>T	XP_011533946.1:p.His6926Tyr
XM_011535645.1:c.20269C>T	XP_011533947.1:p.His6757Tyr
XM_011535647.1:c.15736C>T	XP_011533949.1:p.His5246Tyr
XM_006715408.2:c.22489C>T	XP_006715471.1:p.His7497Tyr
XM_006715410.2:c.22501C>T	XP_006715473.1:p.His7501Tyr
XM_006715412.2:c.22486C>T	XP_006715475.1:p.His7496Tyr
XM_006715413.2:c.22501C>T	XP_006715476.1:p.His7501Tyr
XM_006715415.2:c.22501C>T	XP_006715478.1:p.His7501Tyr
XM_006715416.2:c.22486C>T	XP_006715479.1:p.His7496Tyr
XM_006715417.2:c.22360C>T	XP_006715480.1:p.His7454Tyr
XM_006715420.2:c.22348C>T	XP_006715483.1:p.His7450Tyr
XM_006715421.2:c.22345C>T	XP_006715484.1:p.His7449Tyr
XM_006715423.2:c.22501C>T	XP_006715486.1:p.His7501Tyr
XM_006715424.2:c.22501C>T	XP_006715487.1:p.His7501Tyr
XM_006715425.2:c.22501C>T	XP_006715488.1:p.His7501Tyr
XM_011535641.2:c.22498C>T	XP_011533943.1:p.His7500Tyr
XM_011535642.2:c.22486C>T	XP_011533944.1:p.His7496Tyr
XM_011535645.2:c.20269C>T	XP_011533947.1:p.His6757Tyr
XM_017010608.1:c.22501C>T	XP_016866097.1:p.His7501Tyr
XM_017010609.1:c.22501C>T	XP_016866098.1:p.His7501Tyr
XM_017010610.1:c.22480C>T	XP_016866099.1:p.His7494Tyr
XM_017010611.2:c.22474C>T	XP_016866100.1:p.His7492Tyr
XM_017010612.1:c.22423C>T	XP_016866101.1:p.His7475Tyr
XM_017010613.1:c.22498C>T	XP_016866102.1:p.His7500Tyr
XM_017010614.1:c.22345C>T	XP_016866103.1:p.His7449Tyr
XM_017010615.1:c.22345C>T	XP_016866104.1:p.His7449Tyr
XM_017010616.1:c.22501C>T	XP_016866105.1:p.His7501Tyr
XM_017010617.1:c.22498C>T	XP_016866106.1:p.His7500Tyr
XM_017010618.1:c.22486C>T	XP_016866107.1:p.His7496Tyr
XM_017010619.1:c.20776C>T	XP_016866108.1:p.His6926Tyr
NM_182961.4:c.22465C>T MANE Select	NP_892006.3:p.His7489Tyr
NM_033071.5:c.22252C>T	NP_149062.2:p.His7418Tyr