Canonical Allele Identifier: CA375773671

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712560A>T (hg19) ; chr9:g.137818108A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818108A>T , CM000671.2:g.137818108A>T	GRCh38
NC_000009.11:g.140712560A>T , CM000671.1:g.140712560A>T	GRCh37
NC_000009.10:g.139832381A>T	NCBI36
NG_011776.1:g.204117A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3510A>T MANE Select	ENSP00000417980.1:p.Glu1170Asp
ENST00000636472.1:n.72A>T
ENST00000637161.1:c.3417A>T	ENSP00000490328.1:p.Glu1139Asp
ENST00000637261.1:c.4084A>T	ENSP00000490815.1:n.4084A>T
ENST00000637748.1:n.491A>T
ENST00000637891.1:c.1584A>T	ENSP00000490907.1:n.1584A>T
ENST00000460843.5:c.3510A>T	ENSP00000417980.1:p.Glu1170Asp
ENST00000462942.3:c.2367A>T	ENSP00000436107.1:p.Glu789Asp
ENST00000475564.5:n.1234A>T
ENST00000494249.5:n.863A>T
NM_024757.4:c.3510A>T	NP_079033.4:p.Glu1170Asp
XM_005266105.3:c.3501A>T	XP_005266162.1:p.Glu1167Asp
XM_005266110.1:c.3417A>T	XP_005266167.1:p.Glu1139Asp
XM_006717288.2:c.3492A>T	XP_006717351.1:p.Glu1164Asp
XM_011519021.1:c.3519A>T	XP_011517323.1:p.Glu1173Asp
XM_011519022.1:c.3516A>T	XP_011517324.1:p.Glu1172Asp
XM_011519023.1:c.3498A>T	XP_011517325.1:p.Glu1166Asp
XM_011519024.1:c.3441A>T	XP_011517326.1:p.Glu1147Asp
XM_011519025.1:c.3417A>T	XP_011517327.1:p.Glu1139Asp
XM_011519026.1:c.3375A>T	XP_011517328.1:p.Glu1125Asp
XM_011519029.1:c.1941A>T	XP_011517331.1:p.Glu647Asp
XM_011519030.1:c.1293A>T	XP_011517332.1:p.Glu431Asp
XM_011519031.1:c.1080A>T	XP_011517333.1:p.Glu360Asp
XM_011519032.1:c.1080A>T	XP_011517334.1:p.Glu360Asp
XM_011519033.1:c.3354A>T	XP_011517335.1:p.Glu1118Asp
XR_930459.1:n.5297-3546T>A
NM_001354263.1:c.3489A>T	NP_001341192.1:p.Glu1163Asp
XM_005266105.5:c.3501A>T	XP_005266162.1:p.Glu1167Asp
XM_011519021.3:c.3519A>T	XP_011517323.1:p.Glu1173Asp
XM_011519022.3:c.3516A>T	XP_011517324.1:p.Glu1172Asp
XM_011519023.3:c.3498A>T	XP_011517325.1:p.Glu1166Asp
XM_011519029.3:c.1941A>T	XP_011517331.1:p.Glu647Asp
XM_011519030.3:c.1293A>T	XP_011517332.1:p.Glu431Asp
XM_017015134.1:c.3495A>T	XP_016870623.1:p.Glu1165Asp
XM_017015136.2:c.3411A>T	XP_016870625.1:p.Glu1137Asp
XM_017015137.1:c.3396A>T	XP_016870626.1:p.Glu1132Asp
XM_017015138.1:c.3396A>T	XP_016870627.1:p.Glu1132Asp
XM_024447674.1:c.3339A>T	XP_024303442.1:p.Glu1113Asp
XM_024447675.1:c.3273A>T	XP_024303443.1:p.Glu1091Asp
XM_024447676.1:c.2634A>T	XP_024303444.1:p.Glu878Asp
XM_024447677.1:c.2634A>T	XP_024303445.1:p.Glu878Asp
XM_024447680.1:c.3252A>T	XP_024303448.1:p.Glu1084Asp
NM_024757.5:c.3510A>T MANE Select	NP_079033.4:p.Glu1170Asp
NM_001354263.2:c.3489A>T	NP_001341192.1:p.Glu1163Asp