Canonical Allele Identifier: CA375776552

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671203T>A (hg19) ; chr9:g.137776751T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776751T>A , CM000671.2:g.137776751T>A	GRCh38
NC_000009.11:g.140671203T>A , CM000671.1:g.140671203T>A	GRCh37
NC_000009.10:g.139791024T>A	NCBI36
NG_011776.1:g.162760T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1925T>A MANE Select	ENSP00000417980.1:p.Ile642Lys
ENST00000636027.1:c.1811T>A	ENSP00000489961.1:p.Ile604Lys
ENST00000637161.1:c.1832T>A	ENSP00000490328.1:p.Ile611Lys
ENST00000637261.1:c.1965T>A	ENSP00000490815.1:n.1965T>A
ENST00000638071.1:c.1552T>A
ENST00000640639.1:c.1094T>A	ENSP00000491823.1:p.Ile365Lys
ENST00000371394.6:c.*1660T>A	ENSP00000485945.1:n.*1660T>A
ENST00000460843.5:c.1925T>A	ENSP00000417980.1:p.Ile642Lys
ENST00000462484.5:c.1925T>A	ENSP00000417328.1:p.Ile642Lys
ENST00000462942.3:c.782T>A	ENSP00000436107.1:p.Ile261Lys
ENST00000465566.2:c.473T>A	ENSP00000486261.1:p.Ile158Lys
ENST00000626603.1:n.1698A>T
NM_001145527.1:c.1925T>A	NP_001138999.1:p.Ile642Lys
NM_024757.4:c.1925T>A	NP_079033.4:p.Ile642Lys
XM_005266105.3:c.1916T>A	XP_005266162.1:p.Ile639Lys
XM_005266110.1:c.1832T>A	XP_005266167.1:p.Ile611Lys
XM_006717288.2:c.1907T>A	XP_006717351.1:p.Ile636Lys
XM_011519021.1:c.1934T>A	XP_011517323.1:p.Ile645Lys
XM_011519022.1:c.1931T>A	XP_011517324.1:p.Ile644Lys
XM_011519023.1:c.1913T>A	XP_011517325.1:p.Ile638Lys
XM_011519024.1:c.1856T>A	XP_011517326.1:p.Ile619Lys
XM_011519025.1:c.1832T>A	XP_011517327.1:p.Ile611Lys
XM_011519026.1:c.1790T>A	XP_011517328.1:p.Ile597Lys
XM_011519027.1:c.1934T>A	XP_011517329.1:p.Ile645Lys
XM_011519028.1:c.1934T>A	XP_011517330.1:p.Ile645Lys
XM_011519029.1:c.356T>A	XP_011517331.1:p.Ile119Lys
XM_011519033.1:c.1769T>A	XP_011517335.1:p.Ile590Lys
NM_001354259.1:c.1832T>A	NP_001341188.1:p.Ile611Lys
NM_001354263.1:c.1904T>A	NP_001341192.1:p.Ile635Lys
XM_005266105.5:c.1916T>A	XP_005266162.1:p.Ile639Lys
XM_011519021.3:c.1934T>A	XP_011517323.1:p.Ile645Lys
XM_011519022.3:c.1931T>A	XP_011517324.1:p.Ile644Lys
XM_011519023.3:c.1913T>A	XP_011517325.1:p.Ile638Lys
XM_011519029.3:c.356T>A	XP_011517331.1:p.Ile119Lys
XM_017015134.1:c.1910T>A	XP_016870623.1:p.Ile637Lys
XM_017015136.2:c.1826T>A	XP_016870625.1:p.Ile609Lys
XM_017015137.1:c.1811T>A	XP_016870626.1:p.Ile604Lys
XM_017015138.1:c.1811T>A	XP_016870627.1:p.Ile604Lys
XM_024447674.1:c.1754T>A	XP_024303442.1:p.Ile585Lys
XM_024447675.1:c.1688T>A	XP_024303443.1:p.Ile563Lys
XM_024447676.1:c.1049T>A	XP_024303444.1:p.Ile350Lys
XM_024447677.1:c.1049T>A	XP_024303445.1:p.Ile350Lys
XM_024447678.1:c.1832T>A	XP_024303446.1:p.Ile611Lys
XM_024447679.1:c.1832T>A	XP_024303447.1:p.Ile611Lys
XM_024447680.1:c.1667T>A	XP_024303448.1:p.Ile556Lys
NM_024757.5:c.1925T>A MANE Select	NP_079033.4:p.Ile642Lys
NM_001145527.2:c.1925T>A	NP_001138999.1:p.Ile642Lys
NM_001354259.2:c.1832T>A	NP_001341188.1:p.Ile611Lys
NM_001354263.2:c.1904T>A	NP_001341192.1:p.Ile635Lys