Canonical Allele Identifier: CA467878180

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707958C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813506C>A , CM000671.2:g.137813506C>A	GRCh38
NC_000009.11:g.140707958C>A , CM000671.1:g.140707958C>A	GRCh37
NC_000009.10:g.139827779C>A	NCBI36
NG_011776.1:g.199515C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3156C>A MANE Select	ENSP00000417980.1:p.Ile1052=
ENST00000637161.1:c.3063C>A	ENSP00000490328.1:p.Ile1021=
ENST00000637261.1:c.3196C>A	ENSP00000490815.1:n.3196C>A
ENST00000637891.1:c.1050C>A	ENSP00000490907.1:p.Ile350=
ENST00000460843.5:c.3156C>A	ENSP00000417980.1:p.Ile1052=
ENST00000462942.3:c.2013C>A	ENSP00000436107.1:p.Ile671=
ENST00000483653.1:n.16C>A
ENST00000488242.2:n.682C>A
NM_024757.4:c.3156C>A	NP_079033.4:p.Ile1052=
XM_005266105.3:c.3147C>A	XP_005266162.1:p.Ile1049=
XM_005266110.1:c.3063C>A	XP_005266167.1:p.Ile1021=
XM_006717288.2:c.3138C>A	XP_006717351.1:p.Ile1046=
XM_011519021.1:c.3165C>A	XP_011517323.1:p.Ile1055=
XM_011519022.1:c.3162C>A	XP_011517324.1:p.Ile1054=
XM_011519023.1:c.3144C>A	XP_011517325.1:p.Ile1048=
XM_011519024.1:c.3087C>A	XP_011517326.1:p.Ile1029=
XM_011519025.1:c.3063C>A	XP_011517327.1:p.Ile1021=
XM_011519026.1:c.3021C>A	XP_011517328.1:p.Ile1007=
XM_011519029.1:c.1587C>A	XP_011517331.1:p.Ile529=
XM_011519030.1:c.939C>A	XP_011517332.1:p.Ile313=
XM_011519031.1:c.726C>A	XP_011517333.1:p.Ile242=
XM_011519032.1:c.726C>A	XP_011517334.1:p.Ile242=
XM_011519033.1:c.3000C>A	XP_011517335.1:p.Ile1000=
NM_001354263.1:c.3135C>A	NP_001341192.1:p.Ile1045=
XM_005266105.5:c.3147C>A	XP_005266162.1:p.Ile1049=
XM_011519021.3:c.3165C>A	XP_011517323.1:p.Ile1055=
XM_011519022.3:c.3162C>A	XP_011517324.1:p.Ile1054=
XM_011519023.3:c.3144C>A	XP_011517325.1:p.Ile1048=
XM_011519029.3:c.1587C>A	XP_011517331.1:p.Ile529=
XM_011519030.3:c.939C>A	XP_011517332.1:p.Ile313=
XM_017015134.1:c.3141C>A	XP_016870623.1:p.Ile1047=
XM_017015136.2:c.3057C>A	XP_016870625.1:p.Ile1019=
XM_017015137.1:c.3042C>A	XP_016870626.1:p.Ile1014=
XM_017015138.1:c.3042C>A	XP_016870627.1:p.Ile1014=
XM_024447674.1:c.2985C>A	XP_024303442.1:p.Ile995=
XM_024447675.1:c.2919C>A	XP_024303443.1:p.Ile973=
XM_024447676.1:c.2280C>A	XP_024303444.1:p.Ile760=
XM_024447677.1:c.2280C>A	XP_024303445.1:p.Ile760=
XM_024447680.1:c.2898C>A	XP_024303448.1:p.Ile966=
NM_024757.5:c.3156C>A MANE Select	NP_079033.4:p.Ile1052=
NM_001354263.2:c.3135C>A	NP_001341192.1:p.Ile1045=