Canonical Allele Identifier: CA375776731

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671230T>A (hg19) ; chr9:g.137776778T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776778T>A , CM000671.2:g.137776778T>A	GRCh38
NC_000009.11:g.140671230T>A , CM000671.1:g.140671230T>A	GRCh37
NC_000009.10:g.139791051T>A	NCBI36
NG_011776.1:g.162787T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1952T>A MANE Select	ENSP00000417980.1:p.Val651Glu
ENST00000636027.1:c.1838T>A	ENSP00000489961.1:p.Val613Glu
ENST00000637161.1:c.1859T>A	ENSP00000490328.1:p.Val620Glu
ENST00000637261.1:c.1992T>A	ENSP00000490815.1:n.1992T>A
ENST00000638071.1:c.1579T>A
ENST00000640639.1:c.1121T>A	ENSP00000491823.1:p.Val374Glu
ENST00000371394.6:c.*1687T>A	ENSP00000485945.1:n.*1687T>A
ENST00000460843.5:c.1952T>A	ENSP00000417980.1:p.Val651Glu
ENST00000462484.5:c.1952T>A	ENSP00000417328.1:p.Val651Glu
ENST00000462942.3:c.809T>A	ENSP00000436107.1:p.Val270Glu
ENST00000465566.2:c.500T>A	ENSP00000486261.1:p.Val167Glu
ENST00000626603.1:n.1671A>T
NM_001145527.1:c.1952T>A	NP_001138999.1:p.Val651Glu
NM_024757.4:c.1952T>A	NP_079033.4:p.Val651Glu
XM_005266105.3:c.1943T>A	XP_005266162.1:p.Val648Glu
XM_005266110.1:c.1859T>A	XP_005266167.1:p.Val620Glu
XM_006717288.2:c.1934T>A	XP_006717351.1:p.Val645Glu
XM_011519021.1:c.1961T>A	XP_011517323.1:p.Val654Glu
XM_011519022.1:c.1958T>A	XP_011517324.1:p.Val653Glu
XM_011519023.1:c.1940T>A	XP_011517325.1:p.Val647Glu
XM_011519024.1:c.1883T>A	XP_011517326.1:p.Val628Glu
XM_011519025.1:c.1859T>A	XP_011517327.1:p.Val620Glu
XM_011519026.1:c.1817T>A	XP_011517328.1:p.Val606Glu
XM_011519027.1:c.1961T>A	XP_011517329.1:p.Val654Glu
XM_011519028.1:c.1961T>A	XP_011517330.1:p.Val654Glu
XM_011519029.1:c.383T>A	XP_011517331.1:p.Val128Glu
XM_011519033.1:c.1796T>A	XP_011517335.1:p.Val599Glu
NM_001354259.1:c.1859T>A	NP_001341188.1:p.Val620Glu
NM_001354263.1:c.1931T>A	NP_001341192.1:p.Val644Glu
XM_005266105.5:c.1943T>A	XP_005266162.1:p.Val648Glu
XM_011519021.3:c.1961T>A	XP_011517323.1:p.Val654Glu
XM_011519022.3:c.1958T>A	XP_011517324.1:p.Val653Glu
XM_011519023.3:c.1940T>A	XP_011517325.1:p.Val647Glu
XM_011519029.3:c.383T>A	XP_011517331.1:p.Val128Glu
XM_017015134.1:c.1937T>A	XP_016870623.1:p.Val646Glu
XM_017015136.2:c.1853T>A	XP_016870625.1:p.Val618Glu
XM_017015137.1:c.1838T>A	XP_016870626.1:p.Val613Glu
XM_017015138.1:c.1838T>A	XP_016870627.1:p.Val613Glu
XM_024447674.1:c.1781T>A	XP_024303442.1:p.Val594Glu
XM_024447675.1:c.1715T>A	XP_024303443.1:p.Val572Glu
XM_024447676.1:c.1076T>A	XP_024303444.1:p.Val359Glu
XM_024447677.1:c.1076T>A	XP_024303445.1:p.Val359Glu
XM_024447678.1:c.1859T>A	XP_024303446.1:p.Val620Glu
XM_024447679.1:c.1859T>A	XP_024303447.1:p.Val620Glu
XM_024447680.1:c.1694T>A	XP_024303448.1:p.Val565Glu
NM_024757.5:c.1952T>A MANE Select	NP_079033.4:p.Val651Glu
NM_001145527.2:c.1952T>A	NP_001138999.1:p.Val651Glu
NM_001354259.2:c.1859T>A	NP_001341188.1:p.Val620Glu
NM_001354263.2:c.1931T>A	NP_001341192.1:p.Val644Glu