Canonical Allele Identifier: CA375775751

Gene: EHMT1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000460843.6:c.1823G>C MANE Select	ENSP00000417980.1:p.Ser608Thr
ENST00000636027.1:c.1709G>C	ENSP00000489961.1:p.Ser570Thr
ENST00000637161.1:c.1730G>C	ENSP00000490328.1:p.Ser577Thr
ENST00000637261.1:c.1863G>C	ENSP00000490815.1:n.1863G>C
ENST00000638071.1:c.1450G>C
ENST00000640639.1:c.992G>C	ENSP00000491823.1:p.Ser331Thr
ENST00000371394.6:c.*1558G>C	ENSP00000485945.1:n.*1558G>C
ENST00000460843.5:c.1823G>C	ENSP00000417980.1:p.Ser608Thr
ENST00000462484.5:c.1823G>C	ENSP00000417328.1:p.Ser608Thr
ENST00000462942.3:c.680G>C	ENSP00000436107.1:p.Ser227Thr
ENST00000465566.2:c.371G>C	ENSP00000486261.1:p.Ser124Thr
ENST00000626603.1:n.1800C>G
NM_001145527.1:c.1823G>C	NP_001138999.1:p.Ser608Thr
NM_024757.4:c.1823G>C	NP_079033.4:p.Ser608Thr
XM_005266105.3:c.1814G>C	XP_005266162.1:p.Ser605Thr
XM_005266110.1:c.1730G>C	XP_005266167.1:p.Ser577Thr
XM_006717288.2:c.1805G>C	XP_006717351.1:p.Ser602Thr
XM_011519021.1:c.1832G>C	XP_011517323.1:p.Ser611Thr
XM_011519022.1:c.1829G>C	XP_011517324.1:p.Ser610Thr
XM_011519023.1:c.1811G>C	XP_011517325.1:p.Ser604Thr
XM_011519024.1:c.1754G>C	XP_011517326.1:p.Ser585Thr
XM_011519025.1:c.1730G>C	XP_011517327.1:p.Ser577Thr
XM_011519026.1:c.1688G>C	XP_011517328.1:p.Ser563Thr
XM_011519027.1:c.1832G>C	XP_011517329.1:p.Ser611Thr
XM_011519028.1:c.1832G>C	XP_011517330.1:p.Ser611Thr
XM_011519029.1:c.254G>C	XP_011517331.1:p.Ser85Thr
XM_011519033.1:c.1667G>C	XP_011517335.1:p.Ser556Thr
NM_001354259.1:c.1730G>C	NP_001341188.1:p.Ser577Thr
NM_001354263.1:c.1802G>C	NP_001341192.1:p.Ser601Thr
XM_005266105.5:c.1814G>C	XP_005266162.1:p.Ser605Thr
XM_011519021.3:c.1832G>C	XP_011517323.1:p.Ser611Thr
XM_011519022.3:c.1829G>C	XP_011517324.1:p.Ser610Thr
XM_011519023.3:c.1811G>C	XP_011517325.1:p.Ser604Thr
XM_011519029.3:c.254G>C	XP_011517331.1:p.Ser85Thr
XM_017015134.1:c.1808G>C	XP_016870623.1:p.Ser603Thr
XM_017015136.2:c.1724G>C	XP_016870625.1:p.Ser575Thr
XM_017015137.1:c.1709G>C	XP_016870626.1:p.Ser570Thr
XM_017015138.1:c.1709G>C	XP_016870627.1:p.Ser570Thr
XM_024447674.1:c.1652G>C	XP_024303442.1:p.Ser551Thr
XM_024447675.1:c.1586G>C	XP_024303443.1:p.Ser529Thr
XM_024447676.1:c.947G>C	XP_024303444.1:p.Ser316Thr
XM_024447677.1:c.947G>C	XP_024303445.1:p.Ser316Thr
XM_024447678.1:c.1730G>C	XP_024303446.1:p.Ser577Thr
XM_024447679.1:c.1730G>C	XP_024303447.1:p.Ser577Thr
XM_024447680.1:c.1565G>C	XP_024303448.1:p.Ser522Thr
NM_024757.5:c.1823G>C MANE Select	NP_079033.4:p.Ser608Thr
NM_001145527.2:c.1823G>C	NP_001138999.1:p.Ser608Thr
NM_001354259.2:c.1730G>C	NP_001341188.1:p.Ser577Thr
NM_001354263.2:c.1802G>C	NP_001341192.1:p.Ser601Thr