Canonical Allele Identifier: CA375776811

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671245G>C (hg19) ; chr9:g.137776793G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776793G>C , CM000671.2:g.137776793G>C	GRCh38
NC_000009.11:g.140671245G>C , CM000671.1:g.140671245G>C	GRCh37
NC_000009.10:g.139791066G>C	NCBI36
NG_011776.1:g.162802G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1967G>C MANE Select	ENSP00000417980.1:p.Gly656Ala
ENST00000636027.1:c.1853G>C	ENSP00000489961.1:p.Gly618Ala
ENST00000637161.1:c.1874G>C	ENSP00000490328.1:p.Gly625Ala
ENST00000637261.1:c.2007G>C	ENSP00000490815.1:n.2007G>C
ENST00000638071.1:c.1594G>C
ENST00000640639.1:c.1136G>C	ENSP00000491823.1:p.Gly379Ala
ENST00000371394.6:c.*1702G>C	ENSP00000485945.1:n.*1702G>C
ENST00000460843.5:c.1967G>C	ENSP00000417980.1:p.Gly656Ala
ENST00000462484.5:c.1967G>C	ENSP00000417328.1:p.Gly656Ala
ENST00000462942.3:c.824G>C	ENSP00000436107.1:p.Gly275Ala
ENST00000626603.1:n.1656C>G
NM_001145527.1:c.1967G>C	NP_001138999.1:p.Gly656Ala
NM_024757.4:c.1967G>C	NP_079033.4:p.Gly656Ala
XM_005266105.3:c.1958G>C	XP_005266162.1:p.Gly653Ala
XM_005266110.1:c.1874G>C	XP_005266167.1:p.Gly625Ala
XM_006717288.2:c.1949G>C	XP_006717351.1:p.Gly650Ala
XM_011519021.1:c.1976G>C	XP_011517323.1:p.Gly659Ala
XM_011519022.1:c.1973G>C	XP_011517324.1:p.Gly658Ala
XM_011519023.1:c.1955G>C	XP_011517325.1:p.Gly652Ala
XM_011519024.1:c.1898G>C	XP_011517326.1:p.Gly633Ala
XM_011519025.1:c.1874G>C	XP_011517327.1:p.Gly625Ala
XM_011519026.1:c.1832G>C	XP_011517328.1:p.Gly611Ala
XM_011519027.1:c.1976G>C	XP_011517329.1:p.Gly659Ala
XM_011519028.1:c.1976G>C	XP_011517330.1:p.Gly659Ala
XM_011519029.1:c.398G>C	XP_011517331.1:p.Gly133Ala
XM_011519033.1:c.1811G>C	XP_011517335.1:p.Gly604Ala
NM_001354259.1:c.1874G>C	NP_001341188.1:p.Gly625Ala
NM_001354263.1:c.1946G>C	NP_001341192.1:p.Gly649Ala
XM_005266105.5:c.1958G>C	XP_005266162.1:p.Gly653Ala
XM_011519021.3:c.1976G>C	XP_011517323.1:p.Gly659Ala
XM_011519022.3:c.1973G>C	XP_011517324.1:p.Gly658Ala
XM_011519023.3:c.1955G>C	XP_011517325.1:p.Gly652Ala
XM_011519029.3:c.398G>C	XP_011517331.1:p.Gly133Ala
XM_017015134.1:c.1952G>C	XP_016870623.1:p.Gly651Ala
XM_017015136.2:c.1868G>C	XP_016870625.1:p.Gly623Ala
XM_017015137.1:c.1853G>C	XP_016870626.1:p.Gly618Ala
XM_017015138.1:c.1853G>C	XP_016870627.1:p.Gly618Ala
XM_024447674.1:c.1796G>C	XP_024303442.1:p.Gly599Ala
XM_024447675.1:c.1730G>C	XP_024303443.1:p.Gly577Ala
XM_024447676.1:c.1091G>C	XP_024303444.1:p.Gly364Ala
XM_024447677.1:c.1091G>C	XP_024303445.1:p.Gly364Ala
XM_024447678.1:c.1874G>C	XP_024303446.1:p.Gly625Ala
XM_024447679.1:c.1874G>C	XP_024303447.1:p.Gly625Ala
XM_024447680.1:c.1709G>C	XP_024303448.1:p.Gly570Ala
NM_024757.5:c.1967G>C MANE Select	NP_079033.4:p.Gly656Ala
NM_001145527.2:c.1967G>C	NP_001138999.1:p.Gly656Ala
NM_001354259.2:c.1874G>C	NP_001341188.1:p.Gly625Ala
NM_001354263.2:c.1946G>C	NP_001341192.1:p.Gly649Ala