Canonical Allele Identifier: CA375775585
Gene: EHMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137776635T>G , CM000671.2:g.137776635T>G GRCh38
NC_000009.11:g.140671087T>G , CM000671.1:g.140671087T>G GRCh37
NC_000009.10:g.139790908T>G NCBI36
NG_011776.1:g.162644T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.1809T>G MANE Select ENSP00000417980.1:p.Cys603Trp
ENST00000636027.1:c.1695T>G ENSP00000489961.1:p.Cys565Trp
ENST00000637161.1:c.1716T>G ENSP00000490328.1:p.Cys572Trp
ENST00000637261.1:c.1849T>G ENSP00000490815.1:n.1849T>G
ENST00000638071.1:c.1436T>G
ENST00000640639.1:c.978T>G ENSP00000491823.1:p.Cys326Trp
ENST00000371394.6:c.*1544T>G ENSP00000485945.1:n.*1544T>G
ENST00000460843.5:c.1809T>G ENSP00000417980.1:p.Cys603Trp
ENST00000462484.5:c.1809T>G ENSP00000417328.1:p.Cys603Trp
ENST00000462942.3:c.666T>G ENSP00000436107.1:p.Cys222Trp
ENST00000465566.2:c.357T>G ENSP00000486261.1:p.Cys119Trp
ENST00000626603.1:n.1814A>C
NM_001145527.1:c.1809T>G NP_001138999.1:p.Cys603Trp
NM_024757.4:c.1809T>G NP_079033.4:p.Cys603Trp
XM_005266105.3:c.1800T>G XP_005266162.1:p.Cys600Trp
XM_005266110.1:c.1716T>G XP_005266167.1:p.Cys572Trp
XM_006717288.2:c.1791T>G XP_006717351.1:p.Cys597Trp
XM_011519021.1:c.1818T>G XP_011517323.1:p.Cys606Trp
XM_011519022.1:c.1815T>G XP_011517324.1:p.Cys605Trp
XM_011519023.1:c.1797T>G XP_011517325.1:p.Cys599Trp
XM_011519024.1:c.1740T>G XP_011517326.1:p.Cys580Trp
XM_011519025.1:c.1716T>G XP_011517327.1:p.Cys572Trp
XM_011519026.1:c.1674T>G XP_011517328.1:p.Cys558Trp
XM_011519027.1:c.1818T>G XP_011517329.1:p.Cys606Trp
XM_011519028.1:c.1818T>G XP_011517330.1:p.Cys606Trp
XM_011519029.1:c.240T>G XP_011517331.1:p.Cys80Trp
XM_011519033.1:c.1653T>G XP_011517335.1:p.Cys551Trp
NM_001354259.1:c.1716T>G NP_001341188.1:p.Cys572Trp
NM_001354263.1:c.1788T>G NP_001341192.1:p.Cys596Trp
XM_005266105.5:c.1800T>G XP_005266162.1:p.Cys600Trp
XM_011519021.3:c.1818T>G XP_011517323.1:p.Cys606Trp
XM_011519022.3:c.1815T>G XP_011517324.1:p.Cys605Trp
XM_011519023.3:c.1797T>G XP_011517325.1:p.Cys599Trp
XM_011519029.3:c.240T>G XP_011517331.1:p.Cys80Trp
XM_017015134.1:c.1794T>G XP_016870623.1:p.Cys598Trp
XM_017015136.2:c.1710T>G XP_016870625.1:p.Cys570Trp
XM_017015137.1:c.1695T>G XP_016870626.1:p.Cys565Trp
XM_017015138.1:c.1695T>G XP_016870627.1:p.Cys565Trp
XM_024447674.1:c.1638T>G XP_024303442.1:p.Cys546Trp
XM_024447675.1:c.1572T>G XP_024303443.1:p.Cys524Trp
XM_024447676.1:c.933T>G XP_024303444.1:p.Cys311Trp
XM_024447677.1:c.933T>G XP_024303445.1:p.Cys311Trp
XM_024447678.1:c.1716T>G XP_024303446.1:p.Cys572Trp
XM_024447679.1:c.1716T>G XP_024303447.1:p.Cys572Trp
XM_024447680.1:c.1551T>G XP_024303448.1:p.Cys517Trp
NM_024757.5:c.1809T>G MANE Select NP_079033.4:p.Cys603Trp
NM_001145527.2:c.1809T>G NP_001138999.1:p.Cys603Trp
NM_001354259.2:c.1716T>G NP_001341188.1:p.Cys572Trp
NM_001354263.2:c.1788T>G NP_001341192.1:p.Cys596Trp