Canonical Allele Identifier: CA375777063

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671293G>C (hg19) ; chr9:g.137776841G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776841G>C , CM000671.2:g.137776841G>C	GRCh38
NC_000009.11:g.140671293G>C , CM000671.1:g.140671293G>C	GRCh37
NC_000009.10:g.139791114G>C	NCBI36
NG_011776.1:g.162850G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2015G>C MANE Select	ENSP00000417980.1:p.Gly672Ala
ENST00000636027.1:c.1901G>C	ENSP00000489961.1:p.Gly634Ala
ENST00000637161.1:c.1922G>C	ENSP00000490328.1:p.Gly641Ala
ENST00000637261.1:c.2055G>C	ENSP00000490815.1:n.2055G>C
ENST00000638071.1:c.1642G>C
ENST00000371394.6:c.*1750G>C	ENSP00000485945.1:n.*1750G>C
ENST00000460843.5:c.2015G>C	ENSP00000417980.1:p.Gly672Ala
ENST00000462484.5:c.2015G>C	ENSP00000417328.1:p.Gly672Ala
ENST00000462942.3:c.872G>C	ENSP00000436107.1:p.Gly291Ala
ENST00000626603.1:n.1608C>G
NM_001145527.1:c.2015G>C	NP_001138999.1:p.Gly672Ala
NM_024757.4:c.2015G>C	NP_079033.4:p.Gly672Ala
XM_005266105.3:c.2006G>C	XP_005266162.1:p.Gly669Ala
XM_005266110.1:c.1922G>C	XP_005266167.1:p.Gly641Ala
XM_006717288.2:c.1997G>C	XP_006717351.1:p.Gly666Ala
XM_011519021.1:c.2024G>C	XP_011517323.1:p.Gly675Ala
XM_011519022.1:c.2021G>C	XP_011517324.1:p.Gly674Ala
XM_011519023.1:c.2003G>C	XP_011517325.1:p.Gly668Ala
XM_011519024.1:c.1946G>C	XP_011517326.1:p.Gly649Ala
XM_011519025.1:c.1922G>C	XP_011517327.1:p.Gly641Ala
XM_011519026.1:c.1880G>C	XP_011517328.1:p.Gly627Ala
XM_011519027.1:c.2024G>C	XP_011517329.1:p.Gly675Ala
XM_011519028.1:c.2024G>C	XP_011517330.1:p.Gly675Ala
XM_011519029.1:c.446G>C	XP_011517331.1:p.Gly149Ala
XM_011519033.1:c.1859G>C	XP_011517335.1:p.Gly620Ala
NM_001354259.1:c.1922G>C	NP_001341188.1:p.Gly641Ala
NM_001354263.1:c.1994G>C	NP_001341192.1:p.Gly665Ala
XM_005266105.5:c.2006G>C	XP_005266162.1:p.Gly669Ala
XM_011519021.3:c.2024G>C	XP_011517323.1:p.Gly675Ala
XM_011519022.3:c.2021G>C	XP_011517324.1:p.Gly674Ala
XM_011519023.3:c.2003G>C	XP_011517325.1:p.Gly668Ala
XM_011519029.3:c.446G>C	XP_011517331.1:p.Gly149Ala
XM_017015134.1:c.2000G>C	XP_016870623.1:p.Gly667Ala
XM_017015136.2:c.1916G>C	XP_016870625.1:p.Gly639Ala
XM_017015137.1:c.1901G>C	XP_016870626.1:p.Gly634Ala
XM_017015138.1:c.1901G>C	XP_016870627.1:p.Gly634Ala
XM_024447674.1:c.1844G>C	XP_024303442.1:p.Gly615Ala
XM_024447675.1:c.1778G>C	XP_024303443.1:p.Gly593Ala
XM_024447676.1:c.1139G>C	XP_024303444.1:p.Gly380Ala
XM_024447677.1:c.1139G>C	XP_024303445.1:p.Gly380Ala
XM_024447678.1:c.1922G>C	XP_024303446.1:p.Gly641Ala
XM_024447679.1:c.1922G>C	XP_024303447.1:p.Gly641Ala
XM_024447680.1:c.1757G>C	XP_024303448.1:p.Gly586Ala
NM_024757.5:c.2015G>C MANE Select	NP_079033.4:p.Gly672Ala
NM_001145527.2:c.2015G>C	NP_001138999.1:p.Gly672Ala
NM_001354259.2:c.1922G>C	NP_001341188.1:p.Gly641Ala
NM_001354263.2:c.1994G>C	NP_001341192.1:p.Gly665Ala