Canonical Allele Identifier: CA375776905

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671262G>C (hg19) ; chr9:g.137776810G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776810G>C , CM000671.2:g.137776810G>C	GRCh38
NC_000009.11:g.140671262G>C , CM000671.1:g.140671262G>C	GRCh37
NC_000009.10:g.139791083G>C	NCBI36
NG_011776.1:g.162819G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1984G>C MANE Select	ENSP00000417980.1:p.Ala662Pro
ENST00000636027.1:c.1870G>C	ENSP00000489961.1:p.Ala624Pro
ENST00000637161.1:c.1891G>C	ENSP00000490328.1:p.Ala631Pro
ENST00000637261.1:c.2024G>C	ENSP00000490815.1:n.2024G>C
ENST00000638071.1:c.1611G>C
ENST00000640639.1:c.1153G>C	ENSP00000491823.1:p.Ala385Pro
ENST00000371394.6:c.*1719G>C	ENSP00000485945.1:n.*1719G>C
ENST00000460843.5:c.1984G>C	ENSP00000417980.1:p.Ala662Pro
ENST00000462484.5:c.1984G>C	ENSP00000417328.1:p.Ala662Pro
ENST00000462942.3:c.841G>C	ENSP00000436107.1:p.Ala281Pro
ENST00000626603.1:n.1639C>G
NM_001145527.1:c.1984G>C	NP_001138999.1:p.Ala662Pro
NM_024757.4:c.1984G>C	NP_079033.4:p.Ala662Pro
XM_005266105.3:c.1975G>C	XP_005266162.1:p.Ala659Pro
XM_005266110.1:c.1891G>C	XP_005266167.1:p.Ala631Pro
XM_006717288.2:c.1966G>C	XP_006717351.1:p.Ala656Pro
XM_011519021.1:c.1993G>C	XP_011517323.1:p.Ala665Pro
XM_011519022.1:c.1990G>C	XP_011517324.1:p.Ala664Pro
XM_011519023.1:c.1972G>C	XP_011517325.1:p.Ala658Pro
XM_011519024.1:c.1915G>C	XP_011517326.1:p.Ala639Pro
XM_011519025.1:c.1891G>C	XP_011517327.1:p.Ala631Pro
XM_011519026.1:c.1849G>C	XP_011517328.1:p.Ala617Pro
XM_011519027.1:c.1993G>C	XP_011517329.1:p.Ala665Pro
XM_011519028.1:c.1993G>C	XP_011517330.1:p.Ala665Pro
XM_011519029.1:c.415G>C	XP_011517331.1:p.Ala139Pro
XM_011519033.1:c.1828G>C	XP_011517335.1:p.Ala610Pro
NM_001354259.1:c.1891G>C	NP_001341188.1:p.Ala631Pro
NM_001354263.1:c.1963G>C	NP_001341192.1:p.Ala655Pro
XM_005266105.5:c.1975G>C	XP_005266162.1:p.Ala659Pro
XM_011519021.3:c.1993G>C	XP_011517323.1:p.Ala665Pro
XM_011519022.3:c.1990G>C	XP_011517324.1:p.Ala664Pro
XM_011519023.3:c.1972G>C	XP_011517325.1:p.Ala658Pro
XM_011519029.3:c.415G>C	XP_011517331.1:p.Ala139Pro
XM_017015134.1:c.1969G>C	XP_016870623.1:p.Ala657Pro
XM_017015136.2:c.1885G>C	XP_016870625.1:p.Ala629Pro
XM_017015137.1:c.1870G>C	XP_016870626.1:p.Ala624Pro
XM_017015138.1:c.1870G>C	XP_016870627.1:p.Ala624Pro
XM_024447674.1:c.1813G>C	XP_024303442.1:p.Ala605Pro
XM_024447675.1:c.1747G>C	XP_024303443.1:p.Ala583Pro
XM_024447676.1:c.1108G>C	XP_024303444.1:p.Ala370Pro
XM_024447677.1:c.1108G>C	XP_024303445.1:p.Ala370Pro
XM_024447678.1:c.1891G>C	XP_024303446.1:p.Ala631Pro
XM_024447679.1:c.1891G>C	XP_024303447.1:p.Ala631Pro
XM_024447680.1:c.1726G>C	XP_024303448.1:p.Ala576Pro
NM_024757.5:c.1984G>C MANE Select	NP_079033.4:p.Ala662Pro
NM_001145527.2:c.1984G>C	NP_001138999.1:p.Ala662Pro
NM_001354259.2:c.1891G>C	NP_001341188.1:p.Ala631Pro
NM_001354263.2:c.1963G>C	NP_001341192.1:p.Ala655Pro