Canonical Allele Identifier: CA467873827

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140652447G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137757995G>A , CM000671.2:g.137757995G>A	GRCh38
NC_000009.11:g.140652447G>A , CM000671.1:g.140652447G>A	GRCh37
NC_000009.10:g.139772268G>A	NCBI36
NG_011776.1:g.144004G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1485G>A MANE Select	ENSP00000417980.1:p.Leu495=
ENST00000629335.2:c.1485G>A	ENSP00000490056.1:p.Leu495=
ENST00000636027.1:c.1371G>A	ENSP00000489961.1:p.Leu457=
ENST00000637161.1:c.1392G>A	ENSP00000490328.1:p.Leu464=
ENST00000637261.1:c.1525G>A	ENSP00000490815.1:n.1525G>A
ENST00000637977.1:c.1430G>A
ENST00000638071.1:c.1112G>A
ENST00000640639.1:c.654G>A	ENSP00000491823.1:p.Leu218=
ENST00000371394.6:c.*1220G>A	ENSP00000485945.1:n.*1220G>A
ENST00000460843.5:c.1485G>A	ENSP00000417980.1:p.Leu495=
ENST00000462484.5:c.1485G>A	ENSP00000417328.1:p.Leu495=
ENST00000462942.3:c.342G>A	ENSP00000436107.1:p.Leu114=
ENST00000465566.2:c.177G>A	ENSP00000486261.1:p.Leu59=
ENST00000629808.2:c.578G>A
NM_001145527.1:c.1485G>A	NP_001138999.1:p.Leu495=
NM_024757.4:c.1485G>A	NP_079033.4:p.Leu495=
XM_005266105.3:c.1476G>A	XP_005266162.1:p.Leu492=
XM_005266110.1:c.1392G>A	XP_005266167.1:p.Leu464=
XM_006717288.2:c.1467G>A	XP_006717351.1:p.Leu489=
XM_011519021.1:c.1494G>A	XP_011517323.1:p.Leu498=
XM_011519022.1:c.1491G>A	XP_011517324.1:p.Leu497=
XM_011519023.1:c.1473G>A	XP_011517325.1:p.Leu491=
XM_011519024.1:c.1416G>A	XP_011517326.1:p.Leu472=
XM_011519025.1:c.1392G>A	XP_011517327.1:p.Leu464=
XM_011519026.1:c.1494G>A	XP_011517328.1:p.Leu498=
XM_011519027.1:c.1494G>A	XP_011517329.1:p.Leu498=
XM_011519028.1:c.1494G>A	XP_011517330.1:p.Leu498=
XM_011519033.1:c.1473G>A	XP_011517335.1:p.Leu491=
NM_001354259.1:c.1392G>A	NP_001341188.1:p.Leu464=
NM_001354263.1:c.1464G>A	NP_001341192.1:p.Leu488=
NM_001354611.1:c.1485G>A	NP_001341540.1:p.Leu495=
NM_001354612.1:c.1392G>A	NP_001341541.1:p.Leu464=
XM_005266105.5:c.1476G>A	XP_005266162.1:p.Leu492=
XM_011519021.3:c.1494G>A	XP_011517323.1:p.Leu498=
XM_011519022.3:c.1491G>A	XP_011517324.1:p.Leu497=
XM_011519023.3:c.1473G>A	XP_011517325.1:p.Leu491=
XM_017015134.1:c.1470G>A	XP_016870623.1:p.Leu490=
XM_017015136.2:c.1386G>A	XP_016870625.1:p.Leu462=
XM_017015137.1:c.1371G>A	XP_016870626.1:p.Leu457=
XM_017015138.1:c.1371G>A	XP_016870627.1:p.Leu457=
XM_024447674.1:c.1314G>A	XP_024303442.1:p.Leu438=
XM_024447675.1:c.1392G>A	XP_024303443.1:p.Leu464=
XM_024447676.1:c.609G>A	XP_024303444.1:p.Leu203=
XM_024447677.1:c.609G>A	XP_024303445.1:p.Leu203=
XM_024447678.1:c.1392G>A	XP_024303446.1:p.Leu464=
XM_024447679.1:c.1392G>A	XP_024303447.1:p.Leu464=
XM_024447680.1:c.1371G>A	XP_024303448.1:p.Leu457=
NM_024757.5:c.1485G>A MANE Select	NP_079033.4:p.Leu495=
NM_001145527.2:c.1485G>A	NP_001138999.1:p.Leu495=
NM_001354259.2:c.1392G>A	NP_001341188.1:p.Leu464=
NM_001354263.2:c.1464G>A	NP_001341192.1:p.Leu488=
NM_001354611.2:c.1485G>A	NP_001341540.1:p.Leu495=
NM_001354612.2:c.1392G>A	NP_001341541.1:p.Leu464=