Canonical Allele Identifier: CA861200977
Gene: EHMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1169678743

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137776300_137776301del , CM000671.2:g.137776300_137776301del GRCh38
NC_000009.11:g.140670752_140670753del , CM000671.1:g.140670752_140670753del GRCh37
NC_000009.10:g.139790573_139790574del NCBI36
NG_011776.1:g.162309_162310del

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.1792-318_1792-317del MANE Select ENSP00000417980.1:n.1792-318_1792-317del
ENST00000636027.1:c.1678-318_1678-317del ENSP00000489961.1:n.1678-318_1678-317del
ENST00000637161.1:c.1699-318_1699-317del ENSP00000490328.1:n.1699-318_1699-317del
ENST00000637261.1:c.1832-318_1832-317del ENSP00000490815.1:n.1832-318_1832-317del
ENST00000638071.1:c.1419-318_1419-317del
ENST00000640639.1:c.961-318_961-317del ENSP00000491823.1:n.961-318_961-317del
ENST00000371394.6:c.*1527-318_*1527-317del ENSP00000485945.1:n.*1527-318_*1527-317del
ENST00000460843.5:c.1792-318_1792-317del ENSP00000417980.1:n.1792-318_1792-317del
ENST00000462484.5:c.1792-318_1792-317del ENSP00000417328.1:n.1792-318_1792-317del
ENST00000462942.3:c.649-318_649-317del ENSP00000436107.1:n.649-318_649-317del
ENST00000465566.2:c.340-318_340-317del ENSP00000486261.1:n.340-318_340-317del
NM_001145527.1:c.1792-318_1792-317del NP_001138999.1:n.1792-318_1792-317del
NM_024757.4:c.1792-318_1792-317del NP_079033.4:n.1792-318_1792-317del
XM_005266105.3:c.1783-318_1783-317del XP_005266162.1:n.1783-318_1783-317del
XM_005266110.1:c.1699-318_1699-317del XP_005266167.1:n.1699-318_1699-317del
XM_006717288.2:c.1774-318_1774-317del XP_006717351.1:n.1774-318_1774-317del
XM_011519021.1:c.1801-318_1801-317del XP_011517323.1:n.1801-318_1801-317del
XM_011519022.1:c.1798-318_1798-317del XP_011517324.1:n.1798-318_1798-317del
XM_011519023.1:c.1780-318_1780-317del XP_011517325.1:n.1780-318_1780-317del
XM_011519024.1:c.1723-318_1723-317del XP_011517326.1:n.1723-318_1723-317del
XM_011519025.1:c.1699-318_1699-317del XP_011517327.1:n.1699-318_1699-317del
XM_011519026.1:c.1657-318_1657-317del XP_011517328.1:n.1657-318_1657-317del
XM_011519027.1:c.1801-318_1801-317del XP_011517329.1:n.1801-318_1801-317del
XM_011519028.1:c.1801-318_1801-317del XP_011517330.1:n.1801-318_1801-317del
XM_011519029.1:c.223-318_223-317del XP_011517331.1:n.223-318_223-317del
XM_011519033.1:c.1636-318_1636-317del XP_011517335.1:n.1636-318_1636-317del
NM_001354259.1:c.1699-318_1699-317del NP_001341188.1:n.1699-318_1699-317del
NM_001354263.1:c.1771-318_1771-317del NP_001341192.1:n.1771-318_1771-317del
XM_005266105.5:c.1783-318_1783-317del XP_005266162.1:n.1783-318_1783-317del
XM_011519021.3:c.1801-318_1801-317del XP_011517323.1:n.1801-318_1801-317del
XM_011519022.3:c.1798-318_1798-317del XP_011517324.1:n.1798-318_1798-317del
XM_011519023.3:c.1780-318_1780-317del XP_011517325.1:n.1780-318_1780-317del
XM_011519029.3:c.223-318_223-317del XP_011517331.1:n.223-318_223-317del
XM_017015134.1:c.1777-318_1777-317del XP_016870623.1:n.1777-318_1777-317del
XM_017015136.2:c.1693-318_1693-317del XP_016870625.1:n.1693-318_1693-317del
XM_017015137.1:c.1678-318_1678-317del XP_016870626.1:n.1678-318_1678-317del
XM_017015138.1:c.1678-318_1678-317del XP_016870627.1:n.1678-318_1678-317del
XM_024447674.1:c.1621-318_1621-317del XP_024303442.1:n.1621-318_1621-317del
XM_024447675.1:c.1555-318_1555-317del XP_024303443.1:n.1555-318_1555-317del
XM_024447676.1:c.916-318_916-317del XP_024303444.1:n.916-318_916-317del
XM_024447677.1:c.916-318_916-317del XP_024303445.1:n.916-318_916-317del
XM_024447678.1:c.1699-318_1699-317del XP_024303446.1:n.1699-318_1699-317del
XM_024447679.1:c.1699-318_1699-317del XP_024303447.1:n.1699-318_1699-317del
XM_024447680.1:c.1534-318_1534-317del XP_024303448.1:n.1534-318_1534-317del
NM_024757.5:c.1792-318_1792-317del MANE Select NP_079033.4:n.1792-318_1792-317del
NM_001145527.2:c.1792-318_1792-317del NP_001138999.1:n.1792-318_1792-317del
NM_001354259.2:c.1699-318_1699-317del NP_001341188.1:n.1699-318_1699-317del
NM_001354263.2:c.1771-318_1771-317del NP_001341192.1:n.1771-318_1771-317del