Canonical Allele Identifier: CA375773668

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712559A>T (hg19) ; chr9:g.137818107A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818107A>T , CM000671.2:g.137818107A>T	GRCh38
NC_000009.11:g.140712559A>T , CM000671.1:g.140712559A>T	GRCh37
NC_000009.10:g.139832380A>T	NCBI36
NG_011776.1:g.204116A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3509A>T MANE Select	ENSP00000417980.1:p.Glu1170Val
ENST00000636472.1:n.71A>T
ENST00000637161.1:c.3416A>T	ENSP00000490328.1:p.Glu1139Val
ENST00000637261.1:c.4083A>T	ENSP00000490815.1:n.4083A>T
ENST00000637748.1:n.490A>T
ENST00000637891.1:c.1583A>T	ENSP00000490907.1:n.1583A>T
ENST00000460843.5:c.3509A>T	ENSP00000417980.1:p.Glu1170Val
ENST00000462942.3:c.2366A>T	ENSP00000436107.1:p.Glu789Val
ENST00000475564.5:n.1233A>T
ENST00000494249.5:n.862A>T
NM_024757.4:c.3509A>T	NP_079033.4:p.Glu1170Val
XM_005266105.3:c.3500A>T	XP_005266162.1:p.Glu1167Val
XM_005266110.1:c.3416A>T	XP_005266167.1:p.Glu1139Val
XM_006717288.2:c.3491A>T	XP_006717351.1:p.Glu1164Val
XM_011519021.1:c.3518A>T	XP_011517323.1:p.Glu1173Val
XM_011519022.1:c.3515A>T	XP_011517324.1:p.Glu1172Val
XM_011519023.1:c.3497A>T	XP_011517325.1:p.Glu1166Val
XM_011519024.1:c.3440A>T	XP_011517326.1:p.Glu1147Val
XM_011519025.1:c.3416A>T	XP_011517327.1:p.Glu1139Val
XM_011519026.1:c.3374A>T	XP_011517328.1:p.Glu1125Val
XM_011519029.1:c.1940A>T	XP_011517331.1:p.Glu647Val
XM_011519030.1:c.1292A>T	XP_011517332.1:p.Glu431Val
XM_011519031.1:c.1079A>T	XP_011517333.1:p.Glu360Val
XM_011519032.1:c.1079A>T	XP_011517334.1:p.Glu360Val
XM_011519033.1:c.3353A>T	XP_011517335.1:p.Glu1118Val
XR_930459.1:n.5297-3545T>A
NM_001354263.1:c.3488A>T	NP_001341192.1:p.Glu1163Val
XM_005266105.5:c.3500A>T	XP_005266162.1:p.Glu1167Val
XM_011519021.3:c.3518A>T	XP_011517323.1:p.Glu1173Val
XM_011519022.3:c.3515A>T	XP_011517324.1:p.Glu1172Val
XM_011519023.3:c.3497A>T	XP_011517325.1:p.Glu1166Val
XM_011519029.3:c.1940A>T	XP_011517331.1:p.Glu647Val
XM_011519030.3:c.1292A>T	XP_011517332.1:p.Glu431Val
XM_017015134.1:c.3494A>T	XP_016870623.1:p.Glu1165Val
XM_017015136.2:c.3410A>T	XP_016870625.1:p.Glu1137Val
XM_017015137.1:c.3395A>T	XP_016870626.1:p.Glu1132Val
XM_017015138.1:c.3395A>T	XP_016870627.1:p.Glu1132Val
XM_024447674.1:c.3338A>T	XP_024303442.1:p.Glu1113Val
XM_024447675.1:c.3272A>T	XP_024303443.1:p.Glu1091Val
XM_024447676.1:c.2633A>T	XP_024303444.1:p.Glu878Val
XM_024447677.1:c.2633A>T	XP_024303445.1:p.Glu878Val
XM_024447680.1:c.3251A>T	XP_024303448.1:p.Glu1084Val
NM_024757.5:c.3509A>T MANE Select	NP_079033.4:p.Glu1170Val
NM_001354263.2:c.3488A>T	NP_001341192.1:p.Glu1163Val