Canonical Allele Identifier: CA467878186

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707973T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813521T>A , CM000671.2:g.137813521T>A	GRCh38
NC_000009.11:g.140707973T>A , CM000671.1:g.140707973T>A	GRCh37
NC_000009.10:g.139827794T>A	NCBI36
NG_011776.1:g.199530T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3171T>A MANE Select	ENSP00000417980.1:p.Thr1057=
ENST00000637161.1:c.3078T>A	ENSP00000490328.1:p.Thr1026=
ENST00000637261.1:c.3211T>A	ENSP00000490815.1:n.3211T>A
ENST00000637891.1:c.1065T>A	ENSP00000490907.1:p.Thr355=
ENST00000460843.5:c.3171T>A	ENSP00000417980.1:p.Thr1057=
ENST00000462942.3:c.2028T>A	ENSP00000436107.1:p.Thr676=
ENST00000483653.1:n.31T>A
ENST00000488242.2:n.697T>A
NM_024757.4:c.3171T>A	NP_079033.4:p.Thr1057=
XM_005266105.3:c.3162T>A	XP_005266162.1:p.Thr1054=
XM_005266110.1:c.3078T>A	XP_005266167.1:p.Thr1026=
XM_006717288.2:c.3153T>A	XP_006717351.1:p.Thr1051=
XM_011519021.1:c.3180T>A	XP_011517323.1:p.Thr1060=
XM_011519022.1:c.3177T>A	XP_011517324.1:p.Thr1059=
XM_011519023.1:c.3159T>A	XP_011517325.1:p.Thr1053=
XM_011519024.1:c.3102T>A	XP_011517326.1:p.Thr1034=
XM_011519025.1:c.3078T>A	XP_011517327.1:p.Thr1026=
XM_011519026.1:c.3036T>A	XP_011517328.1:p.Thr1012=
XM_011519029.1:c.1602T>A	XP_011517331.1:p.Thr534=
XM_011519030.1:c.954T>A	XP_011517332.1:p.Thr318=
XM_011519031.1:c.741T>A	XP_011517333.1:p.Thr247=
XM_011519032.1:c.741T>A	XP_011517334.1:p.Thr247=
XM_011519033.1:c.3015T>A	XP_011517335.1:p.Thr1005=
NM_001354263.1:c.3150T>A	NP_001341192.1:p.Thr1050=
XM_005266105.5:c.3162T>A	XP_005266162.1:p.Thr1054=
XM_011519021.3:c.3180T>A	XP_011517323.1:p.Thr1060=
XM_011519022.3:c.3177T>A	XP_011517324.1:p.Thr1059=
XM_011519023.3:c.3159T>A	XP_011517325.1:p.Thr1053=
XM_011519029.3:c.1602T>A	XP_011517331.1:p.Thr534=
XM_011519030.3:c.954T>A	XP_011517332.1:p.Thr318=
XM_017015134.1:c.3156T>A	XP_016870623.1:p.Thr1052=
XM_017015136.2:c.3072T>A	XP_016870625.1:p.Thr1024=
XM_017015137.1:c.3057T>A	XP_016870626.1:p.Thr1019=
XM_017015138.1:c.3057T>A	XP_016870627.1:p.Thr1019=
XM_024447674.1:c.3000T>A	XP_024303442.1:p.Thr1000=
XM_024447675.1:c.2934T>A	XP_024303443.1:p.Thr978=
XM_024447676.1:c.2295T>A	XP_024303444.1:p.Thr765=
XM_024447677.1:c.2295T>A	XP_024303445.1:p.Thr765=
XM_024447680.1:c.2913T>A	XP_024303448.1:p.Thr971=
NM_024757.5:c.3171T>A MANE Select	NP_079033.4:p.Thr1057=
NM_001354263.2:c.3150T>A	NP_001341192.1:p.Thr1050=