Canonical Allele Identifier: CA467874037

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671072T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776620T>A , CM000671.2:g.137776620T>A	GRCh38
NC_000009.11:g.140671072T>A , CM000671.1:g.140671072T>A	GRCh37
NC_000009.10:g.139790893T>A	NCBI36
NG_011776.1:g.162629T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1794T>A MANE Select	ENSP00000417980.1:p.Gly598=
ENST00000636027.1:c.1680T>A	ENSP00000489961.1:p.Gly560=
ENST00000637161.1:c.1701T>A	ENSP00000490328.1:p.Gly567=
ENST00000637261.1:c.1834T>A	ENSP00000490815.1:n.1834T>A
ENST00000638071.1:c.1421T>A
ENST00000640639.1:c.963T>A	ENSP00000491823.1:p.Gly321=
ENST00000371394.6:c.*1529T>A	ENSP00000485945.1:n.*1529T>A
ENST00000460843.5:c.1794T>A	ENSP00000417980.1:p.Gly598=
ENST00000462484.5:c.1794T>A	ENSP00000417328.1:p.Gly598=
ENST00000462942.3:c.651T>A	ENSP00000436107.1:p.Gly217=
ENST00000465566.2:c.342T>A	ENSP00000486261.1:p.Gly114=
ENST00000626603.1:n.1829A>T
NM_001145527.1:c.1794T>A	NP_001138999.1:p.Gly598=
NM_024757.4:c.1794T>A	NP_079033.4:p.Gly598=
XM_005266105.3:c.1785T>A	XP_005266162.1:p.Gly595=
XM_005266110.1:c.1701T>A	XP_005266167.1:p.Gly567=
XM_006717288.2:c.1776T>A	XP_006717351.1:p.Gly592=
XM_011519021.1:c.1803T>A	XP_011517323.1:p.Gly601=
XM_011519022.1:c.1800T>A	XP_011517324.1:p.Gly600=
XM_011519023.1:c.1782T>A	XP_011517325.1:p.Gly594=
XM_011519024.1:c.1725T>A	XP_011517326.1:p.Gly575=
XM_011519025.1:c.1701T>A	XP_011517327.1:p.Gly567=
XM_011519026.1:c.1659T>A	XP_011517328.1:p.Gly553=
XM_011519027.1:c.1803T>A	XP_011517329.1:p.Gly601=
XM_011519028.1:c.1803T>A	XP_011517330.1:p.Gly601=
XM_011519029.1:c.225T>A	XP_011517331.1:p.Gly75=
XM_011519033.1:c.1638T>A	XP_011517335.1:p.Gly546=
NM_001354259.1:c.1701T>A	NP_001341188.1:p.Gly567=
NM_001354263.1:c.1773T>A	NP_001341192.1:p.Gly591=
XM_005266105.5:c.1785T>A	XP_005266162.1:p.Gly595=
XM_011519021.3:c.1803T>A	XP_011517323.1:p.Gly601=
XM_011519022.3:c.1800T>A	XP_011517324.1:p.Gly600=
XM_011519023.3:c.1782T>A	XP_011517325.1:p.Gly594=
XM_011519029.3:c.225T>A	XP_011517331.1:p.Gly75=
XM_017015134.1:c.1779T>A	XP_016870623.1:p.Gly593=
XM_017015136.2:c.1695T>A	XP_016870625.1:p.Gly565=
XM_017015137.1:c.1680T>A	XP_016870626.1:p.Gly560=
XM_017015138.1:c.1680T>A	XP_016870627.1:p.Gly560=
XM_024447674.1:c.1623T>A	XP_024303442.1:p.Gly541=
XM_024447675.1:c.1557T>A	XP_024303443.1:p.Gly519=
XM_024447676.1:c.918T>A	XP_024303444.1:p.Gly306=
XM_024447677.1:c.918T>A	XP_024303445.1:p.Gly306=
XM_024447678.1:c.1701T>A	XP_024303446.1:p.Gly567=
XM_024447679.1:c.1701T>A	XP_024303447.1:p.Gly567=
XM_024447680.1:c.1536T>A	XP_024303448.1:p.Gly512=
NM_024757.5:c.1794T>A MANE Select	NP_079033.4:p.Gly598=
NM_001145527.2:c.1794T>A	NP_001138999.1:p.Gly598=
NM_001354259.2:c.1701T>A	NP_001341188.1:p.Gly567=
NM_001354263.2:c.1773T>A	NP_001341192.1:p.Gly591=