Canonical Allele Identifier: CA375775772

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671106T>G (hg19) ; chr9:g.137776654T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776654T>G , CM000671.2:g.137776654T>G	GRCh38
NC_000009.11:g.140671106T>G , CM000671.1:g.140671106T>G	GRCh37
NC_000009.10:g.139790927T>G	NCBI36
NG_011776.1:g.162663T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1828T>G MANE Select	ENSP00000417980.1:p.Ser610Ala
ENST00000636027.1:c.1714T>G	ENSP00000489961.1:p.Ser572Ala
ENST00000637161.1:c.1735T>G	ENSP00000490328.1:p.Ser579Ala
ENST00000637261.1:c.1868T>G	ENSP00000490815.1:n.1868T>G
ENST00000638071.1:c.1455T>G
ENST00000640639.1:c.997T>G	ENSP00000491823.1:p.Ser333Ala
ENST00000371394.6:c.*1563T>G	ENSP00000485945.1:n.*1563T>G
ENST00000460843.5:c.1828T>G	ENSP00000417980.1:p.Ser610Ala
ENST00000462484.5:c.1828T>G	ENSP00000417328.1:p.Ser610Ala
ENST00000462942.3:c.685T>G	ENSP00000436107.1:p.Ser229Ala
ENST00000465566.2:c.376T>G	ENSP00000486261.1:p.Ser126Ala
ENST00000626603.1:n.1795A>C
NM_001145527.1:c.1828T>G	NP_001138999.1:p.Ser610Ala
NM_024757.4:c.1828T>G	NP_079033.4:p.Ser610Ala
XM_005266105.3:c.1819T>G	XP_005266162.1:p.Ser607Ala
XM_005266110.1:c.1735T>G	XP_005266167.1:p.Ser579Ala
XM_006717288.2:c.1810T>G	XP_006717351.1:p.Ser604Ala
XM_011519021.1:c.1837T>G	XP_011517323.1:p.Ser613Ala
XM_011519022.1:c.1834T>G	XP_011517324.1:p.Ser612Ala
XM_011519023.1:c.1816T>G	XP_011517325.1:p.Ser606Ala
XM_011519024.1:c.1759T>G	XP_011517326.1:p.Ser587Ala
XM_011519025.1:c.1735T>G	XP_011517327.1:p.Ser579Ala
XM_011519026.1:c.1693T>G	XP_011517328.1:p.Ser565Ala
XM_011519027.1:c.1837T>G	XP_011517329.1:p.Ser613Ala
XM_011519028.1:c.1837T>G	XP_011517330.1:p.Ser613Ala
XM_011519029.1:c.259T>G	XP_011517331.1:p.Ser87Ala
XM_011519033.1:c.1672T>G	XP_011517335.1:p.Ser558Ala
NM_001354259.1:c.1735T>G	NP_001341188.1:p.Ser579Ala
NM_001354263.1:c.1807T>G	NP_001341192.1:p.Ser603Ala
XM_005266105.5:c.1819T>G	XP_005266162.1:p.Ser607Ala
XM_011519021.3:c.1837T>G	XP_011517323.1:p.Ser613Ala
XM_011519022.3:c.1834T>G	XP_011517324.1:p.Ser612Ala
XM_011519023.3:c.1816T>G	XP_011517325.1:p.Ser606Ala
XM_011519029.3:c.259T>G	XP_011517331.1:p.Ser87Ala
XM_017015134.1:c.1813T>G	XP_016870623.1:p.Ser605Ala
XM_017015136.2:c.1729T>G	XP_016870625.1:p.Ser577Ala
XM_017015137.1:c.1714T>G	XP_016870626.1:p.Ser572Ala
XM_017015138.1:c.1714T>G	XP_016870627.1:p.Ser572Ala
XM_024447674.1:c.1657T>G	XP_024303442.1:p.Ser553Ala
XM_024447675.1:c.1591T>G	XP_024303443.1:p.Ser531Ala
XM_024447676.1:c.952T>G	XP_024303444.1:p.Ser318Ala
XM_024447677.1:c.952T>G	XP_024303445.1:p.Ser318Ala
XM_024447678.1:c.1735T>G	XP_024303446.1:p.Ser579Ala
XM_024447679.1:c.1735T>G	XP_024303447.1:p.Ser579Ala
XM_024447680.1:c.1570T>G	XP_024303448.1:p.Ser524Ala
NM_024757.5:c.1828T>G MANE Select	NP_079033.4:p.Ser610Ala
NM_001145527.2:c.1828T>G	NP_001138999.1:p.Ser610Ala
NM_001354259.2:c.1735T>G	NP_001341188.1:p.Ser579Ala
NM_001354263.2:c.1807T>G	NP_001341192.1:p.Ser603Ala