Canonical Allele Identifier: CA375775732

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671100A>C (hg19) ; chr9:g.137776648A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776648A>C , CM000671.2:g.137776648A>C	GRCh38
NC_000009.11:g.140671100A>C , CM000671.1:g.140671100A>C	GRCh37
NC_000009.10:g.139790921A>C	NCBI36
NG_011776.1:g.162657A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000460843.6:c.1822A>C MANE Select	ENSP00000417980.1:p.Ser608Arg
ENST00000636027.1:c.1708A>C	ENSP00000489961.1:p.Ser570Arg
ENST00000637161.1:c.1729A>C	ENSP00000490328.1:p.Ser577Arg
ENST00000637261.1:c.1862A>C	ENSP00000490815.1:n.1862A>C
ENST00000638071.1:c.1449A>C
ENST00000640639.1:c.991A>C	ENSP00000491823.1:p.Ser331Arg
ENST00000371394.6:c.*1557A>C	ENSP00000485945.1:n.*1557A>C
ENST00000460843.5:c.1822A>C	ENSP00000417980.1:p.Ser608Arg
ENST00000462484.5:c.1822A>C	ENSP00000417328.1:p.Ser608Arg
ENST00000462942.3:c.679A>C	ENSP00000436107.1:p.Ser227Arg
ENST00000465566.2:c.370A>C	ENSP00000486261.1:p.Ser124Arg
ENST00000626603.1:n.1801T>G
NM_001145527.1:c.1822A>C	NP_001138999.1:p.Ser608Arg
NM_024757.4:c.1822A>C	NP_079033.4:p.Ser608Arg
XM_005266105.3:c.1813A>C	XP_005266162.1:p.Ser605Arg
XM_005266110.1:c.1729A>C	XP_005266167.1:p.Ser577Arg
XM_006717288.2:c.1804A>C	XP_006717351.1:p.Ser602Arg
XM_011519021.1:c.1831A>C	XP_011517323.1:p.Ser611Arg
XM_011519022.1:c.1828A>C	XP_011517324.1:p.Ser610Arg
XM_011519023.1:c.1810A>C	XP_011517325.1:p.Ser604Arg
XM_011519024.1:c.1753A>C	XP_011517326.1:p.Ser585Arg
XM_011519025.1:c.1729A>C	XP_011517327.1:p.Ser577Arg
XM_011519026.1:c.1687A>C	XP_011517328.1:p.Ser563Arg
XM_011519027.1:c.1831A>C	XP_011517329.1:p.Ser611Arg
XM_011519028.1:c.1831A>C	XP_011517330.1:p.Ser611Arg
XM_011519029.1:c.253A>C	XP_011517331.1:p.Ser85Arg
XM_011519033.1:c.1666A>C	XP_011517335.1:p.Ser556Arg
NM_001354259.1:c.1729A>C	NP_001341188.1:p.Ser577Arg
NM_001354263.1:c.1801A>C	NP_001341192.1:p.Ser601Arg
XM_005266105.5:c.1813A>C	XP_005266162.1:p.Ser605Arg
XM_011519021.3:c.1831A>C	XP_011517323.1:p.Ser611Arg
XM_011519022.3:c.1828A>C	XP_011517324.1:p.Ser610Arg
XM_011519023.3:c.1810A>C	XP_011517325.1:p.Ser604Arg
XM_011519029.3:c.253A>C	XP_011517331.1:p.Ser85Arg
XM_017015134.1:c.1807A>C	XP_016870623.1:p.Ser603Arg
XM_017015136.2:c.1723A>C	XP_016870625.1:p.Ser575Arg
XM_017015137.1:c.1708A>C	XP_016870626.1:p.Ser570Arg
XM_017015138.1:c.1708A>C	XP_016870627.1:p.Ser570Arg
XM_024447674.1:c.1651A>C	XP_024303442.1:p.Ser551Arg
XM_024447675.1:c.1585A>C	XP_024303443.1:p.Ser529Arg
XM_024447676.1:c.946A>C	XP_024303444.1:p.Ser316Arg
XM_024447677.1:c.946A>C	XP_024303445.1:p.Ser316Arg
XM_024447678.1:c.1729A>C	XP_024303446.1:p.Ser577Arg
XM_024447679.1:c.1729A>C	XP_024303447.1:p.Ser577Arg
XM_024447680.1:c.1564A>C	XP_024303448.1:p.Ser522Arg
NM_024757.5:c.1822A>C MANE Select	NP_079033.4:p.Ser608Arg
NM_001145527.2:c.1822A>C	NP_001138999.1:p.Ser608Arg
NM_001354259.2:c.1729A>C	NP_001341188.1:p.Ser577Arg
NM_001354263.2:c.1801A>C	NP_001341192.1:p.Ser601Arg