Canonical Allele Identifier: CA861201050
Gene: EHMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1457832634

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137776511_137776512del , CM000671.2:g.137776511_137776512del GRCh38
NC_000009.11:g.140670963_140670964del , CM000671.1:g.140670963_140670964del GRCh37
NC_000009.10:g.139790784_139790785del NCBI36
NG_011776.1:g.162520_162521del

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.1792-107_1792-106del MANE Select ENSP00000417980.1:n.1792-107_1792-106del
ENST00000636027.1:c.1678-107_1678-106del ENSP00000489961.1:n.1678-107_1678-106del
ENST00000637161.1:c.1699-107_1699-106del ENSP00000490328.1:n.1699-107_1699-106del
ENST00000637261.1:c.1832-107_1832-106del ENSP00000490815.1:n.1832-107_1832-106del
ENST00000638071.1:c.1419-107_1419-106del
ENST00000640639.1:c.961-107_961-106del ENSP00000491823.1:n.961-107_961-106del
ENST00000371394.6:c.*1527-107_*1527-106del ENSP00000485945.1:n.*1527-107_*1527-106del
ENST00000460843.5:c.1792-107_1792-106del ENSP00000417980.1:n.1792-107_1792-106del
ENST00000462484.5:c.1792-107_1792-106del ENSP00000417328.1:n.1792-107_1792-106del
ENST00000462942.3:c.649-107_649-106del ENSP00000436107.1:n.649-107_649-106del
ENST00000465566.2:c.340-107_340-106del ENSP00000486261.1:n.340-107_340-106del
NM_001145527.1:c.1792-107_1792-106del NP_001138999.1:n.1792-107_1792-106del
NM_024757.4:c.1792-107_1792-106del NP_079033.4:n.1792-107_1792-106del
XM_005266105.3:c.1783-107_1783-106del XP_005266162.1:n.1783-107_1783-106del
XM_005266110.1:c.1699-107_1699-106del XP_005266167.1:n.1699-107_1699-106del
XM_006717288.2:c.1774-107_1774-106del XP_006717351.1:n.1774-107_1774-106del
XM_011519021.1:c.1801-107_1801-106del XP_011517323.1:n.1801-107_1801-106del
XM_011519022.1:c.1798-107_1798-106del XP_011517324.1:n.1798-107_1798-106del
XM_011519023.1:c.1780-107_1780-106del XP_011517325.1:n.1780-107_1780-106del
XM_011519024.1:c.1723-107_1723-106del XP_011517326.1:n.1723-107_1723-106del
XM_011519025.1:c.1699-107_1699-106del XP_011517327.1:n.1699-107_1699-106del
XM_011519026.1:c.1657-107_1657-106del XP_011517328.1:n.1657-107_1657-106del
XM_011519027.1:c.1801-107_1801-106del XP_011517329.1:n.1801-107_1801-106del
XM_011519028.1:c.1801-107_1801-106del XP_011517330.1:n.1801-107_1801-106del
XM_011519029.1:c.223-107_223-106del XP_011517331.1:n.223-107_223-106del
XM_011519033.1:c.1636-107_1636-106del XP_011517335.1:n.1636-107_1636-106del
NM_001354259.1:c.1699-107_1699-106del NP_001341188.1:n.1699-107_1699-106del
NM_001354263.1:c.1771-107_1771-106del NP_001341192.1:n.1771-107_1771-106del
XM_005266105.5:c.1783-107_1783-106del XP_005266162.1:n.1783-107_1783-106del
XM_011519021.3:c.1801-107_1801-106del XP_011517323.1:n.1801-107_1801-106del
XM_011519022.3:c.1798-107_1798-106del XP_011517324.1:n.1798-107_1798-106del
XM_011519023.3:c.1780-107_1780-106del XP_011517325.1:n.1780-107_1780-106del
XM_011519029.3:c.223-107_223-106del XP_011517331.1:n.223-107_223-106del
XM_017015134.1:c.1777-107_1777-106del XP_016870623.1:n.1777-107_1777-106del
XM_017015136.2:c.1693-107_1693-106del XP_016870625.1:n.1693-107_1693-106del
XM_017015137.1:c.1678-107_1678-106del XP_016870626.1:n.1678-107_1678-106del
XM_017015138.1:c.1678-107_1678-106del XP_016870627.1:n.1678-107_1678-106del
XM_024447674.1:c.1621-107_1621-106del XP_024303442.1:n.1621-107_1621-106del
XM_024447675.1:c.1555-107_1555-106del XP_024303443.1:n.1555-107_1555-106del
XM_024447676.1:c.916-107_916-106del XP_024303444.1:n.916-107_916-106del
XM_024447677.1:c.916-107_916-106del XP_024303445.1:n.916-107_916-106del
XM_024447678.1:c.1699-107_1699-106del XP_024303446.1:n.1699-107_1699-106del
XM_024447679.1:c.1699-107_1699-106del XP_024303447.1:n.1699-107_1699-106del
XM_024447680.1:c.1534-107_1534-106del XP_024303448.1:n.1534-107_1534-106del
NM_024757.5:c.1792-107_1792-106del MANE Select NP_079033.4:n.1792-107_1792-106del
NM_001145527.2:c.1792-107_1792-106del NP_001138999.1:n.1792-107_1792-106del
NM_001354259.2:c.1699-107_1699-106del NP_001341188.1:n.1699-107_1699-106del
NM_001354263.2:c.1771-107_1771-106del NP_001341192.1:n.1771-107_1771-106del