Canonical Allele Identifier: CA375775737

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671101G>A (hg19) ; chr9:g.137776649G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776649G>A , CM000671.2:g.137776649G>A	GRCh38
NC_000009.11:g.140671101G>A , CM000671.1:g.140671101G>A	GRCh37
NC_000009.10:g.139790922G>A	NCBI36
NG_011776.1:g.162658G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000460843.6:c.1823G>A MANE Select	ENSP00000417980.1:p.Ser608Asn
ENST00000636027.1:c.1709G>A	ENSP00000489961.1:p.Ser570Asn
ENST00000637161.1:c.1730G>A	ENSP00000490328.1:p.Ser577Asn
ENST00000637261.1:c.1863G>A	ENSP00000490815.1:n.1863G>A
ENST00000638071.1:c.1450G>A
ENST00000640639.1:c.992G>A	ENSP00000491823.1:p.Ser331Asn
ENST00000371394.6:c.*1558G>A	ENSP00000485945.1:n.*1558G>A
ENST00000460843.5:c.1823G>A	ENSP00000417980.1:p.Ser608Asn
ENST00000462484.5:c.1823G>A	ENSP00000417328.1:p.Ser608Asn
ENST00000462942.3:c.680G>A	ENSP00000436107.1:p.Ser227Asn
ENST00000465566.2:c.371G>A	ENSP00000486261.1:p.Ser124Asn
ENST00000626603.1:n.1800C>T
NM_001145527.1:c.1823G>A	NP_001138999.1:p.Ser608Asn
NM_024757.4:c.1823G>A	NP_079033.4:p.Ser608Asn
XM_005266105.3:c.1814G>A	XP_005266162.1:p.Ser605Asn
XM_005266110.1:c.1730G>A	XP_005266167.1:p.Ser577Asn
XM_006717288.2:c.1805G>A	XP_006717351.1:p.Ser602Asn
XM_011519021.1:c.1832G>A	XP_011517323.1:p.Ser611Asn
XM_011519022.1:c.1829G>A	XP_011517324.1:p.Ser610Asn
XM_011519023.1:c.1811G>A	XP_011517325.1:p.Ser604Asn
XM_011519024.1:c.1754G>A	XP_011517326.1:p.Ser585Asn
XM_011519025.1:c.1730G>A	XP_011517327.1:p.Ser577Asn
XM_011519026.1:c.1688G>A	XP_011517328.1:p.Ser563Asn
XM_011519027.1:c.1832G>A	XP_011517329.1:p.Ser611Asn
XM_011519028.1:c.1832G>A	XP_011517330.1:p.Ser611Asn
XM_011519029.1:c.254G>A	XP_011517331.1:p.Ser85Asn
XM_011519033.1:c.1667G>A	XP_011517335.1:p.Ser556Asn
NM_001354259.1:c.1730G>A	NP_001341188.1:p.Ser577Asn
NM_001354263.1:c.1802G>A	NP_001341192.1:p.Ser601Asn
XM_005266105.5:c.1814G>A	XP_005266162.1:p.Ser605Asn
XM_011519021.3:c.1832G>A	XP_011517323.1:p.Ser611Asn
XM_011519022.3:c.1829G>A	XP_011517324.1:p.Ser610Asn
XM_011519023.3:c.1811G>A	XP_011517325.1:p.Ser604Asn
XM_011519029.3:c.254G>A	XP_011517331.1:p.Ser85Asn
XM_017015134.1:c.1808G>A	XP_016870623.1:p.Ser603Asn
XM_017015136.2:c.1724G>A	XP_016870625.1:p.Ser575Asn
XM_017015137.1:c.1709G>A	XP_016870626.1:p.Ser570Asn
XM_017015138.1:c.1709G>A	XP_016870627.1:p.Ser570Asn
XM_024447674.1:c.1652G>A	XP_024303442.1:p.Ser551Asn
XM_024447675.1:c.1586G>A	XP_024303443.1:p.Ser529Asn
XM_024447676.1:c.947G>A	XP_024303444.1:p.Ser316Asn
XM_024447677.1:c.947G>A	XP_024303445.1:p.Ser316Asn
XM_024447678.1:c.1730G>A	XP_024303446.1:p.Ser577Asn
XM_024447679.1:c.1730G>A	XP_024303447.1:p.Ser577Asn
XM_024447680.1:c.1565G>A	XP_024303448.1:p.Ser522Asn
NM_024757.5:c.1823G>A MANE Select	NP_079033.4:p.Ser608Asn
NM_001145527.2:c.1823G>A	NP_001138999.1:p.Ser608Asn
NM_001354259.2:c.1730G>A	NP_001341188.1:p.Ser577Asn
NM_001354263.2:c.1802G>A	NP_001341192.1:p.Ser601Asn