Canonical Allele Identifier: CA467874105

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671207T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776755T>G , CM000671.2:g.137776755T>G	GRCh38
NC_000009.11:g.140671207T>G , CM000671.1:g.140671207T>G	GRCh37
NC_000009.10:g.139791028T>G	NCBI36
NG_011776.1:g.162764T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1929T>G MANE Select	ENSP00000417980.1:p.Ala643=
ENST00000636027.1:c.1815T>G	ENSP00000489961.1:p.Ala605=
ENST00000637161.1:c.1836T>G	ENSP00000490328.1:p.Ala612=
ENST00000637261.1:c.1969T>G	ENSP00000490815.1:n.1969T>G
ENST00000638071.1:c.1556T>G
ENST00000640639.1:c.1098T>G	ENSP00000491823.1:p.Ala366=
ENST00000371394.6:c.*1664T>G	ENSP00000485945.1:n.*1664T>G
ENST00000460843.5:c.1929T>G	ENSP00000417980.1:p.Ala643=
ENST00000462484.5:c.1929T>G	ENSP00000417328.1:p.Ala643=
ENST00000462942.3:c.786T>G	ENSP00000436107.1:p.Ala262=
ENST00000465566.2:c.477T>G	ENSP00000486261.1:p.Ala159=
ENST00000626603.1:n.1694A>C
NM_001145527.1:c.1929T>G	NP_001138999.1:p.Ala643=
NM_024757.4:c.1929T>G	NP_079033.4:p.Ala643=
XM_005266105.3:c.1920T>G	XP_005266162.1:p.Ala640=
XM_005266110.1:c.1836T>G	XP_005266167.1:p.Ala612=
XM_006717288.2:c.1911T>G	XP_006717351.1:p.Ala637=
XM_011519021.1:c.1938T>G	XP_011517323.1:p.Ala646=
XM_011519022.1:c.1935T>G	XP_011517324.1:p.Ala645=
XM_011519023.1:c.1917T>G	XP_011517325.1:p.Ala639=
XM_011519024.1:c.1860T>G	XP_011517326.1:p.Ala620=
XM_011519025.1:c.1836T>G	XP_011517327.1:p.Ala612=
XM_011519026.1:c.1794T>G	XP_011517328.1:p.Ala598=
XM_011519027.1:c.1938T>G	XP_011517329.1:p.Ala646=
XM_011519028.1:c.1938T>G	XP_011517330.1:p.Ala646=
XM_011519029.1:c.360T>G	XP_011517331.1:p.Ala120=
XM_011519033.1:c.1773T>G	XP_011517335.1:p.Ala591=
NM_001354259.1:c.1836T>G	NP_001341188.1:p.Ala612=
NM_001354263.1:c.1908T>G	NP_001341192.1:p.Ala636=
XM_005266105.5:c.1920T>G	XP_005266162.1:p.Ala640=
XM_011519021.3:c.1938T>G	XP_011517323.1:p.Ala646=
XM_011519022.3:c.1935T>G	XP_011517324.1:p.Ala645=
XM_011519023.3:c.1917T>G	XP_011517325.1:p.Ala639=
XM_011519029.3:c.360T>G	XP_011517331.1:p.Ala120=
XM_017015134.1:c.1914T>G	XP_016870623.1:p.Ala638=
XM_017015136.2:c.1830T>G	XP_016870625.1:p.Ala610=
XM_017015137.1:c.1815T>G	XP_016870626.1:p.Ala605=
XM_017015138.1:c.1815T>G	XP_016870627.1:p.Ala605=
XM_024447674.1:c.1758T>G	XP_024303442.1:p.Ala586=
XM_024447675.1:c.1692T>G	XP_024303443.1:p.Ala564=
XM_024447676.1:c.1053T>G	XP_024303444.1:p.Ala351=
XM_024447677.1:c.1053T>G	XP_024303445.1:p.Ala351=
XM_024447678.1:c.1836T>G	XP_024303446.1:p.Ala612=
XM_024447679.1:c.1836T>G	XP_024303447.1:p.Ala612=
XM_024447680.1:c.1671T>G	XP_024303448.1:p.Ala557=
NM_024757.5:c.1929T>G MANE Select	NP_079033.4:p.Ala643=
NM_001145527.2:c.1929T>G	NP_001138999.1:p.Ala643=
NM_001354259.2:c.1836T>G	NP_001341188.1:p.Ala612=
NM_001354263.2:c.1908T>G	NP_001341192.1:p.Ala636=