Canonical Allele Identifier: CA375776851

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671252G>T (hg19) ; chr9:g.137776800G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776800G>T , CM000671.2:g.137776800G>T	GRCh38
NC_000009.11:g.140671252G>T , CM000671.1:g.140671252G>T	GRCh37
NC_000009.10:g.139791073G>T	NCBI36
NG_011776.1:g.162809G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1974G>T MANE Select	ENSP00000417980.1:p.Glu658Asp
ENST00000636027.1:c.1860G>T	ENSP00000489961.1:p.Glu620Asp
ENST00000637161.1:c.1881G>T	ENSP00000490328.1:p.Glu627Asp
ENST00000637261.1:c.2014G>T	ENSP00000490815.1:n.2014G>T
ENST00000638071.1:c.1601G>T
ENST00000640639.1:c.1143G>T	ENSP00000491823.1:p.Glu381Asp
ENST00000371394.6:c.*1709G>T	ENSP00000485945.1:n.*1709G>T
ENST00000460843.5:c.1974G>T	ENSP00000417980.1:p.Glu658Asp
ENST00000462484.5:c.1974G>T	ENSP00000417328.1:p.Glu658Asp
ENST00000462942.3:c.831G>T	ENSP00000436107.1:p.Glu277Asp
ENST00000626603.1:n.1649C>A
NM_001145527.1:c.1974G>T	NP_001138999.1:p.Glu658Asp
NM_024757.4:c.1974G>T	NP_079033.4:p.Glu658Asp
XM_005266105.3:c.1965G>T	XP_005266162.1:p.Glu655Asp
XM_005266110.1:c.1881G>T	XP_005266167.1:p.Glu627Asp
XM_006717288.2:c.1956G>T	XP_006717351.1:p.Glu652Asp
XM_011519021.1:c.1983G>T	XP_011517323.1:p.Glu661Asp
XM_011519022.1:c.1980G>T	XP_011517324.1:p.Glu660Asp
XM_011519023.1:c.1962G>T	XP_011517325.1:p.Glu654Asp
XM_011519024.1:c.1905G>T	XP_011517326.1:p.Glu635Asp
XM_011519025.1:c.1881G>T	XP_011517327.1:p.Glu627Asp
XM_011519026.1:c.1839G>T	XP_011517328.1:p.Glu613Asp
XM_011519027.1:c.1983G>T	XP_011517329.1:p.Glu661Asp
XM_011519028.1:c.1983G>T	XP_011517330.1:p.Glu661Asp
XM_011519029.1:c.405G>T	XP_011517331.1:p.Glu135Asp
XM_011519033.1:c.1818G>T	XP_011517335.1:p.Glu606Asp
NM_001354259.1:c.1881G>T	NP_001341188.1:p.Glu627Asp
NM_001354263.1:c.1953G>T	NP_001341192.1:p.Glu651Asp
XM_005266105.5:c.1965G>T	XP_005266162.1:p.Glu655Asp
XM_011519021.3:c.1983G>T	XP_011517323.1:p.Glu661Asp
XM_011519022.3:c.1980G>T	XP_011517324.1:p.Glu660Asp
XM_011519023.3:c.1962G>T	XP_011517325.1:p.Glu654Asp
XM_011519029.3:c.405G>T	XP_011517331.1:p.Glu135Asp
XM_017015134.1:c.1959G>T	XP_016870623.1:p.Glu653Asp
XM_017015136.2:c.1875G>T	XP_016870625.1:p.Glu625Asp
XM_017015137.1:c.1860G>T	XP_016870626.1:p.Glu620Asp
XM_017015138.1:c.1860G>T	XP_016870627.1:p.Glu620Asp
XM_024447674.1:c.1803G>T	XP_024303442.1:p.Glu601Asp
XM_024447675.1:c.1737G>T	XP_024303443.1:p.Glu579Asp
XM_024447676.1:c.1098G>T	XP_024303444.1:p.Glu366Asp
XM_024447677.1:c.1098G>T	XP_024303445.1:p.Glu366Asp
XM_024447678.1:c.1881G>T	XP_024303446.1:p.Glu627Asp
XM_024447679.1:c.1881G>T	XP_024303447.1:p.Glu627Asp
XM_024447680.1:c.1716G>T	XP_024303448.1:p.Glu572Asp
NM_024757.5:c.1974G>T MANE Select	NP_079033.4:p.Glu658Asp
NM_001145527.2:c.1974G>T	NP_001138999.1:p.Glu658Asp
NM_001354259.2:c.1881G>T	NP_001341188.1:p.Glu627Asp
NM_001354263.2:c.1953G>T	NP_001341192.1:p.Glu651Asp