Canonical Allele Identifier: CA468161424

Gene: EHMT1

Linked Data

• gnomAD v4: 9-137813434-C-G
• MyVariant Identifiers: chr9:g.140707886C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813434C>G , CM000671.2:g.137813434C>G	GRCh38
NC_000009.11:g.140707886C>G , CM000671.1:g.140707886C>G	GRCh37
NC_000009.10:g.139827707C>G	NCBI36
NG_011776.1:g.199443C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000460843.6:c.3084C>G MANE Select	ENSP00000417980.1:p.Ala1028=
ENST00000637161.1:c.2991C>G	ENSP00000490328.1:p.Ala997=
ENST00000637261.1:c.3124C>G	ENSP00000490815.1:n.3124C>G
ENST00000637891.1:c.978C>G	ENSP00000490907.1:p.Ala326=
ENST00000460843.5:c.3084C>G	ENSP00000417980.1:p.Ala1028=
ENST00000462942.3:c.1941C>G	ENSP00000436107.1:p.Ala647=
ENST00000486164.5:c.771C>G
ENST00000488242.2:n.610C>G
NM_024757.4:c.3084C>G	NP_079033.4:p.Ala1028=
XM_005266105.3:c.3075C>G	XP_005266162.1:p.Ala1025=
XM_005266110.1:c.2991C>G	XP_005266167.1:p.Ala997=
XM_006717288.2:c.3066C>G	XP_006717351.1:p.Ala1022=
XM_011519021.1:c.3093C>G	XP_011517323.1:p.Ala1031=
XM_011519022.1:c.3090C>G	XP_011517324.1:p.Ala1030=
XM_011519023.1:c.3072C>G	XP_011517325.1:p.Ala1024=
XM_011519024.1:c.3015C>G	XP_011517326.1:p.Ala1005=
XM_011519025.1:c.2991C>G	XP_011517327.1:p.Ala997=
XM_011519026.1:c.2949C>G	XP_011517328.1:p.Ala983=
XM_011519029.1:c.1515C>G	XP_011517331.1:p.Ala505=
XM_011519030.1:c.867C>G	XP_011517332.1:p.Ala289=
XM_011519031.1:c.654C>G	XP_011517333.1:p.Ala218=
XM_011519032.1:c.654C>G	XP_011517334.1:p.Ala218=
XM_011519033.1:c.2928C>G	XP_011517335.1:p.Ala976=
NM_001354263.1:c.3063C>G	NP_001341192.1:p.Ala1021=
XM_005266105.5:c.3075C>G	XP_005266162.1:p.Ala1025=
XM_011519021.3:c.3093C>G	XP_011517323.1:p.Ala1031=
XM_011519022.3:c.3090C>G	XP_011517324.1:p.Ala1030=
XM_011519023.3:c.3072C>G	XP_011517325.1:p.Ala1024=
XM_011519029.3:c.1515C>G	XP_011517331.1:p.Ala505=
XM_011519030.3:c.867C>G	XP_011517332.1:p.Ala289=
XM_017015134.1:c.3069C>G	XP_016870623.1:p.Ala1023=
XM_017015136.2:c.2985C>G	XP_016870625.1:p.Ala995=
XM_017015137.1:c.2970C>G	XP_016870626.1:p.Ala990=
XM_017015138.1:c.2970C>G	XP_016870627.1:p.Ala990=
XM_024447674.1:c.2913C>G	XP_024303442.1:p.Ala971=
XM_024447675.1:c.2847C>G	XP_024303443.1:p.Ala949=
XM_024447676.1:c.2208C>G	XP_024303444.1:p.Ala736=
XM_024447677.1:c.2208C>G	XP_024303445.1:p.Ala736=
XM_024447680.1:c.2826C>G	XP_024303448.1:p.Ala942=
NM_024757.5:c.3084C>G MANE Select	NP_079033.4:p.Ala1028=
NM_001354263.2:c.3063C>G	NP_001341192.1:p.Ala1021=