Canonical Allele Identifier: CA467874139

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671255G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776803G>A , CM000671.2:g.137776803G>A	GRCh38
NC_000009.11:g.140671255G>A , CM000671.1:g.140671255G>A	GRCh37
NC_000009.10:g.139791076G>A	NCBI36
NG_011776.1:g.162812G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1977G>A MANE Select	ENSP00000417980.1:p.Lys659=
ENST00000636027.1:c.1863G>A	ENSP00000489961.1:p.Lys621=
ENST00000637161.1:c.1884G>A	ENSP00000490328.1:p.Lys628=
ENST00000637261.1:c.2017G>A	ENSP00000490815.1:n.2017G>A
ENST00000638071.1:c.1604G>A
ENST00000640639.1:c.1146G>A	ENSP00000491823.1:p.Lys382=
ENST00000371394.6:c.*1712G>A	ENSP00000485945.1:n.*1712G>A
ENST00000460843.5:c.1977G>A	ENSP00000417980.1:p.Lys659=
ENST00000462484.5:c.1977G>A	ENSP00000417328.1:p.Lys659=
ENST00000462942.3:c.834G>A	ENSP00000436107.1:p.Lys278=
ENST00000626603.1:n.1646C>T
NM_001145527.1:c.1977G>A	NP_001138999.1:p.Lys659=
NM_024757.4:c.1977G>A	NP_079033.4:p.Lys659=
XM_005266105.3:c.1968G>A	XP_005266162.1:p.Lys656=
XM_005266110.1:c.1884G>A	XP_005266167.1:p.Lys628=
XM_006717288.2:c.1959G>A	XP_006717351.1:p.Lys653=
XM_011519021.1:c.1986G>A	XP_011517323.1:p.Lys662=
XM_011519022.1:c.1983G>A	XP_011517324.1:p.Lys661=
XM_011519023.1:c.1965G>A	XP_011517325.1:p.Lys655=
XM_011519024.1:c.1908G>A	XP_011517326.1:p.Lys636=
XM_011519025.1:c.1884G>A	XP_011517327.1:p.Lys628=
XM_011519026.1:c.1842G>A	XP_011517328.1:p.Lys614=
XM_011519027.1:c.1986G>A	XP_011517329.1:p.Lys662=
XM_011519028.1:c.1986G>A	XP_011517330.1:p.Lys662=
XM_011519029.1:c.408G>A	XP_011517331.1:p.Lys136=
XM_011519033.1:c.1821G>A	XP_011517335.1:p.Lys607=
NM_001354259.1:c.1884G>A	NP_001341188.1:p.Lys628=
NM_001354263.1:c.1956G>A	NP_001341192.1:p.Lys652=
XM_005266105.5:c.1968G>A	XP_005266162.1:p.Lys656=
XM_011519021.3:c.1986G>A	XP_011517323.1:p.Lys662=
XM_011519022.3:c.1983G>A	XP_011517324.1:p.Lys661=
XM_011519023.3:c.1965G>A	XP_011517325.1:p.Lys655=
XM_011519029.3:c.408G>A	XP_011517331.1:p.Lys136=
XM_017015134.1:c.1962G>A	XP_016870623.1:p.Lys654=
XM_017015136.2:c.1878G>A	XP_016870625.1:p.Lys626=
XM_017015137.1:c.1863G>A	XP_016870626.1:p.Lys621=
XM_017015138.1:c.1863G>A	XP_016870627.1:p.Lys621=
XM_024447674.1:c.1806G>A	XP_024303442.1:p.Lys602=
XM_024447675.1:c.1740G>A	XP_024303443.1:p.Lys580=
XM_024447676.1:c.1101G>A	XP_024303444.1:p.Lys367=
XM_024447677.1:c.1101G>A	XP_024303445.1:p.Lys367=
XM_024447678.1:c.1884G>A	XP_024303446.1:p.Lys628=
XM_024447679.1:c.1884G>A	XP_024303447.1:p.Lys628=
XM_024447680.1:c.1719G>A	XP_024303448.1:p.Lys573=
NM_024757.5:c.1977G>A MANE Select	NP_079033.4:p.Lys659=
NM_001145527.2:c.1977G>A	NP_001138999.1:p.Lys659=
NM_001354259.2:c.1884G>A	NP_001341188.1:p.Lys628=
NM_001354263.2:c.1956G>A	NP_001341192.1:p.Lys652=