Canonical Allele Identifier: CA375773353

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712522G>T (hg19) ; chr9:g.137818070G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818070G>T , CM000671.2:g.137818070G>T	GRCh38
NC_000009.11:g.140712522G>T , CM000671.1:g.140712522G>T	GRCh37
NC_000009.10:g.139832343G>T	NCBI36
NG_011776.1:g.204079G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3472G>T MANE Select	ENSP00000417980.1:p.Glu1158Ter
ENST00000636472.1:n.34G>T
ENST00000637161.1:c.3379G>T	ENSP00000490328.1:p.Glu1127Ter
ENST00000637261.1:c.4046G>T	ENSP00000490815.1:n.4046G>T
ENST00000637748.1:n.453G>T
ENST00000637891.1:c.1546G>T	ENSP00000490907.1:n.1546G>T
ENST00000460843.5:c.3472G>T	ENSP00000417980.1:p.Glu1158Ter
ENST00000462942.3:c.2329G>T	ENSP00000436107.1:p.Glu777Ter
ENST00000475564.5:n.1196G>T
ENST00000494249.5:n.825G>T
NM_024757.4:c.3472G>T	NP_079033.4:p.Glu1158Ter
XM_005266105.3:c.3463G>T	XP_005266162.1:p.Glu1155Ter
XM_005266110.1:c.3379G>T	XP_005266167.1:p.Glu1127Ter
XM_006717288.2:c.3454G>T	XP_006717351.1:p.Glu1152Ter
XM_011519021.1:c.3481G>T	XP_011517323.1:p.Glu1161Ter
XM_011519022.1:c.3478G>T	XP_011517324.1:p.Glu1160Ter
XM_011519023.1:c.3460G>T	XP_011517325.1:p.Glu1154Ter
XM_011519024.1:c.3403G>T	XP_011517326.1:p.Glu1135Ter
XM_011519025.1:c.3379G>T	XP_011517327.1:p.Glu1127Ter
XM_011519026.1:c.3337G>T	XP_011517328.1:p.Glu1113Ter
XM_011519029.1:c.1903G>T	XP_011517331.1:p.Glu635Ter
XM_011519030.1:c.1255G>T	XP_011517332.1:p.Glu419Ter
XM_011519031.1:c.1042G>T	XP_011517333.1:p.Glu348Ter
XM_011519032.1:c.1042G>T	XP_011517334.1:p.Glu348Ter
XM_011519033.1:c.3316G>T	XP_011517335.1:p.Glu1106Ter
XR_930459.1:n.5297-3508C>A
NM_001354263.1:c.3451G>T	NP_001341192.1:p.Glu1151Ter
XM_005266105.5:c.3463G>T	XP_005266162.1:p.Glu1155Ter
XM_011519021.3:c.3481G>T	XP_011517323.1:p.Glu1161Ter
XM_011519022.3:c.3478G>T	XP_011517324.1:p.Glu1160Ter
XM_011519023.3:c.3460G>T	XP_011517325.1:p.Glu1154Ter
XM_011519029.3:c.1903G>T	XP_011517331.1:p.Glu635Ter
XM_011519030.3:c.1255G>T	XP_011517332.1:p.Glu419Ter
XM_017015134.1:c.3457G>T	XP_016870623.1:p.Glu1153Ter
XM_017015136.2:c.3373G>T	XP_016870625.1:p.Glu1125Ter
XM_017015137.1:c.3358G>T	XP_016870626.1:p.Glu1120Ter
XM_017015138.1:c.3358G>T	XP_016870627.1:p.Glu1120Ter
XM_024447674.1:c.3301G>T	XP_024303442.1:p.Glu1101Ter
XM_024447675.1:c.3235G>T	XP_024303443.1:p.Glu1079Ter
XM_024447676.1:c.2596G>T	XP_024303444.1:p.Glu866Ter
XM_024447677.1:c.2596G>T	XP_024303445.1:p.Glu866Ter
XM_024447680.1:c.3214G>T	XP_024303448.1:p.Glu1072Ter
NM_024757.5:c.3472G>T MANE Select	NP_079033.4:p.Glu1158Ter
NM_001354263.2:c.3451G>T	NP_001341192.1:p.Glu1151Ter