Canonical Allele Identifier: CA375775711

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671099C>A (hg19) ; chr9:g.137776647C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776647C>A , CM000671.2:g.137776647C>A	GRCh38
NC_000009.11:g.140671099C>A , CM000671.1:g.140671099C>A	GRCh37
NC_000009.10:g.139790920C>A	NCBI36
NG_011776.1:g.162656C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000460843.6:c.1821C>A MANE Select	ENSP00000417980.1:p.Ser607Arg
ENST00000636027.1:c.1707C>A	ENSP00000489961.1:p.Ser569Arg
ENST00000637161.1:c.1728C>A	ENSP00000490328.1:p.Ser576Arg
ENST00000637261.1:c.1861C>A	ENSP00000490815.1:n.1861C>A
ENST00000638071.1:c.1448C>A
ENST00000640639.1:c.990C>A	ENSP00000491823.1:p.Ser330Arg
ENST00000371394.6:c.*1556C>A	ENSP00000485945.1:n.*1556C>A
ENST00000460843.5:c.1821C>A	ENSP00000417980.1:p.Ser607Arg
ENST00000462484.5:c.1821C>A	ENSP00000417328.1:p.Ser607Arg
ENST00000462942.3:c.678C>A	ENSP00000436107.1:p.Ser226Arg
ENST00000465566.2:c.369C>A	ENSP00000486261.1:p.Ser123Arg
ENST00000626603.1:n.1802G>T
NM_001145527.1:c.1821C>A	NP_001138999.1:p.Ser607Arg
NM_024757.4:c.1821C>A	NP_079033.4:p.Ser607Arg
XM_005266105.3:c.1812C>A	XP_005266162.1:p.Ser604Arg
XM_005266110.1:c.1728C>A	XP_005266167.1:p.Ser576Arg
XM_006717288.2:c.1803C>A	XP_006717351.1:p.Ser601Arg
XM_011519021.1:c.1830C>A	XP_011517323.1:p.Ser610Arg
XM_011519022.1:c.1827C>A	XP_011517324.1:p.Ser609Arg
XM_011519023.1:c.1809C>A	XP_011517325.1:p.Ser603Arg
XM_011519024.1:c.1752C>A	XP_011517326.1:p.Ser584Arg
XM_011519025.1:c.1728C>A	XP_011517327.1:p.Ser576Arg
XM_011519026.1:c.1686C>A	XP_011517328.1:p.Ser562Arg
XM_011519027.1:c.1830C>A	XP_011517329.1:p.Ser610Arg
XM_011519028.1:c.1830C>A	XP_011517330.1:p.Ser610Arg
XM_011519029.1:c.252C>A	XP_011517331.1:p.Ser84Arg
XM_011519033.1:c.1665C>A	XP_011517335.1:p.Ser555Arg
NM_001354259.1:c.1728C>A	NP_001341188.1:p.Ser576Arg
NM_001354263.1:c.1800C>A	NP_001341192.1:p.Ser600Arg
XM_005266105.5:c.1812C>A	XP_005266162.1:p.Ser604Arg
XM_011519021.3:c.1830C>A	XP_011517323.1:p.Ser610Arg
XM_011519022.3:c.1827C>A	XP_011517324.1:p.Ser609Arg
XM_011519023.3:c.1809C>A	XP_011517325.1:p.Ser603Arg
XM_011519029.3:c.252C>A	XP_011517331.1:p.Ser84Arg
XM_017015134.1:c.1806C>A	XP_016870623.1:p.Ser602Arg
XM_017015136.2:c.1722C>A	XP_016870625.1:p.Ser574Arg
XM_017015137.1:c.1707C>A	XP_016870626.1:p.Ser569Arg
XM_017015138.1:c.1707C>A	XP_016870627.1:p.Ser569Arg
XM_024447674.1:c.1650C>A	XP_024303442.1:p.Ser550Arg
XM_024447675.1:c.1584C>A	XP_024303443.1:p.Ser528Arg
XM_024447676.1:c.945C>A	XP_024303444.1:p.Ser315Arg
XM_024447677.1:c.945C>A	XP_024303445.1:p.Ser315Arg
XM_024447678.1:c.1728C>A	XP_024303446.1:p.Ser576Arg
XM_024447679.1:c.1728C>A	XP_024303447.1:p.Ser576Arg
XM_024447680.1:c.1563C>A	XP_024303448.1:p.Ser521Arg
NM_024757.5:c.1821C>A MANE Select	NP_079033.4:p.Ser607Arg
NM_001145527.2:c.1821C>A	NP_001138999.1:p.Ser607Arg
NM_001354259.2:c.1728C>A	NP_001341188.1:p.Ser576Arg
NM_001354263.2:c.1800C>A	NP_001341192.1:p.Ser600Arg