Canonical Allele Identifier: CA467874124

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671231G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776779G>C , CM000671.2:g.137776779G>C	GRCh38
NC_000009.11:g.140671231G>C , CM000671.1:g.140671231G>C	GRCh37
NC_000009.10:g.139791052G>C	NCBI36
NG_011776.1:g.162788G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1953G>C MANE Select	ENSP00000417980.1:p.Val651=
ENST00000636027.1:c.1839G>C	ENSP00000489961.1:p.Val613=
ENST00000637161.1:c.1860G>C	ENSP00000490328.1:p.Val620=
ENST00000637261.1:c.1993G>C	ENSP00000490815.1:n.1993G>C
ENST00000638071.1:c.1580G>C
ENST00000640639.1:c.1122G>C	ENSP00000491823.1:p.Val374=
ENST00000371394.6:c.*1688G>C	ENSP00000485945.1:n.*1688G>C
ENST00000460843.5:c.1953G>C	ENSP00000417980.1:p.Val651=
ENST00000462484.5:c.1953G>C	ENSP00000417328.1:p.Val651=
ENST00000462942.3:c.810G>C	ENSP00000436107.1:p.Val270=
ENST00000465566.2:c.501G>C	ENSP00000486261.1:p.Val167=
ENST00000626603.1:n.1670C>G
NM_001145527.1:c.1953G>C	NP_001138999.1:p.Val651=
NM_024757.4:c.1953G>C	NP_079033.4:p.Val651=
XM_005266105.3:c.1944G>C	XP_005266162.1:p.Val648=
XM_005266110.1:c.1860G>C	XP_005266167.1:p.Val620=
XM_006717288.2:c.1935G>C	XP_006717351.1:p.Val645=
XM_011519021.1:c.1962G>C	XP_011517323.1:p.Val654=
XM_011519022.1:c.1959G>C	XP_011517324.1:p.Val653=
XM_011519023.1:c.1941G>C	XP_011517325.1:p.Val647=
XM_011519024.1:c.1884G>C	XP_011517326.1:p.Val628=
XM_011519025.1:c.1860G>C	XP_011517327.1:p.Val620=
XM_011519026.1:c.1818G>C	XP_011517328.1:p.Val606=
XM_011519027.1:c.1962G>C	XP_011517329.1:p.Val654=
XM_011519028.1:c.1962G>C	XP_011517330.1:p.Val654=
XM_011519029.1:c.384G>C	XP_011517331.1:p.Val128=
XM_011519033.1:c.1797G>C	XP_011517335.1:p.Val599=
NM_001354259.1:c.1860G>C	NP_001341188.1:p.Val620=
NM_001354263.1:c.1932G>C	NP_001341192.1:p.Val644=
XM_005266105.5:c.1944G>C	XP_005266162.1:p.Val648=
XM_011519021.3:c.1962G>C	XP_011517323.1:p.Val654=
XM_011519022.3:c.1959G>C	XP_011517324.1:p.Val653=
XM_011519023.3:c.1941G>C	XP_011517325.1:p.Val647=
XM_011519029.3:c.384G>C	XP_011517331.1:p.Val128=
XM_017015134.1:c.1938G>C	XP_016870623.1:p.Val646=
XM_017015136.2:c.1854G>C	XP_016870625.1:p.Val618=
XM_017015137.1:c.1839G>C	XP_016870626.1:p.Val613=
XM_017015138.1:c.1839G>C	XP_016870627.1:p.Val613=
XM_024447674.1:c.1782G>C	XP_024303442.1:p.Val594=
XM_024447675.1:c.1716G>C	XP_024303443.1:p.Val572=
XM_024447676.1:c.1077G>C	XP_024303444.1:p.Val359=
XM_024447677.1:c.1077G>C	XP_024303445.1:p.Val359=
XM_024447678.1:c.1860G>C	XP_024303446.1:p.Val620=
XM_024447679.1:c.1860G>C	XP_024303447.1:p.Val620=
XM_024447680.1:c.1695G>C	XP_024303448.1:p.Val565=
NM_024757.5:c.1953G>C MANE Select	NP_079033.4:p.Val651=
NM_001145527.2:c.1953G>C	NP_001138999.1:p.Val651=
NM_001354259.2:c.1860G>C	NP_001341188.1:p.Val620=
NM_001354263.2:c.1932G>C	NP_001341192.1:p.Val644=