Canonical Allele Identifier: CA375775694

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671098G>A (hg19) ; chr9:g.137776646G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776646G>A , CM000671.2:g.137776646G>A	GRCh38
NC_000009.11:g.140671098G>A , CM000671.1:g.140671098G>A	GRCh37
NC_000009.10:g.139790919G>A	NCBI36
NG_011776.1:g.162655G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1820G>A MANE Select	ENSP00000417980.1:p.Ser607Asn
ENST00000636027.1:c.1706G>A	ENSP00000489961.1:p.Ser569Asn
ENST00000637161.1:c.1727G>A	ENSP00000490328.1:p.Ser576Asn
ENST00000637261.1:c.1860G>A	ENSP00000490815.1:n.1860G>A
ENST00000638071.1:c.1447G>A
ENST00000640639.1:c.989G>A	ENSP00000491823.1:p.Ser330Asn
ENST00000371394.6:c.*1555G>A	ENSP00000485945.1:n.*1555G>A
ENST00000460843.5:c.1820G>A	ENSP00000417980.1:p.Ser607Asn
ENST00000462484.5:c.1820G>A	ENSP00000417328.1:p.Ser607Asn
ENST00000462942.3:c.677G>A	ENSP00000436107.1:p.Ser226Asn
ENST00000465566.2:c.368G>A	ENSP00000486261.1:p.Ser123Asn
ENST00000626603.1:n.1803C>T
NM_001145527.1:c.1820G>A	NP_001138999.1:p.Ser607Asn
NM_024757.4:c.1820G>A	NP_079033.4:p.Ser607Asn
XM_005266105.3:c.1811G>A	XP_005266162.1:p.Ser604Asn
XM_005266110.1:c.1727G>A	XP_005266167.1:p.Ser576Asn
XM_006717288.2:c.1802G>A	XP_006717351.1:p.Ser601Asn
XM_011519021.1:c.1829G>A	XP_011517323.1:p.Ser610Asn
XM_011519022.1:c.1826G>A	XP_011517324.1:p.Ser609Asn
XM_011519023.1:c.1808G>A	XP_011517325.1:p.Ser603Asn
XM_011519024.1:c.1751G>A	XP_011517326.1:p.Ser584Asn
XM_011519025.1:c.1727G>A	XP_011517327.1:p.Ser576Asn
XM_011519026.1:c.1685G>A	XP_011517328.1:p.Ser562Asn
XM_011519027.1:c.1829G>A	XP_011517329.1:p.Ser610Asn
XM_011519028.1:c.1829G>A	XP_011517330.1:p.Ser610Asn
XM_011519029.1:c.251G>A	XP_011517331.1:p.Ser84Asn
XM_011519033.1:c.1664G>A	XP_011517335.1:p.Ser555Asn
NM_001354259.1:c.1727G>A	NP_001341188.1:p.Ser576Asn
NM_001354263.1:c.1799G>A	NP_001341192.1:p.Ser600Asn
XM_005266105.5:c.1811G>A	XP_005266162.1:p.Ser604Asn
XM_011519021.3:c.1829G>A	XP_011517323.1:p.Ser610Asn
XM_011519022.3:c.1826G>A	XP_011517324.1:p.Ser609Asn
XM_011519023.3:c.1808G>A	XP_011517325.1:p.Ser603Asn
XM_011519029.3:c.251G>A	XP_011517331.1:p.Ser84Asn
XM_017015134.1:c.1805G>A	XP_016870623.1:p.Ser602Asn
XM_017015136.2:c.1721G>A	XP_016870625.1:p.Ser574Asn
XM_017015137.1:c.1706G>A	XP_016870626.1:p.Ser569Asn
XM_017015138.1:c.1706G>A	XP_016870627.1:p.Ser569Asn
XM_024447674.1:c.1649G>A	XP_024303442.1:p.Ser550Asn
XM_024447675.1:c.1583G>A	XP_024303443.1:p.Ser528Asn
XM_024447676.1:c.944G>A	XP_024303444.1:p.Ser315Asn
XM_024447677.1:c.944G>A	XP_024303445.1:p.Ser315Asn
XM_024447678.1:c.1727G>A	XP_024303446.1:p.Ser576Asn
XM_024447679.1:c.1727G>A	XP_024303447.1:p.Ser576Asn
XM_024447680.1:c.1562G>A	XP_024303448.1:p.Ser521Asn
NM_024757.5:c.1820G>A MANE Select	NP_079033.4:p.Ser607Asn
NM_001145527.2:c.1820G>A	NP_001138999.1:p.Ser607Asn
NM_001354259.2:c.1727G>A	NP_001341188.1:p.Ser576Asn
NM_001354263.2:c.1799G>A	NP_001341192.1:p.Ser600Asn