Canonical Allele Identifier: CA1884659436
Gene: EHMT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137762458_137762459delinsAG , CM000671.2:g.137762458_137762459delinsAG GRCh38
NC_000009.11:g.140656910_140656911delinsAG , CM000671.1:g.140656910_140656911delinsAG GRCh37
NC_000009.10:g.139776731_139776732delinsAG NCBI36
NG_011776.1:g.148467_148468delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.1502-217_1502-216delinsAG MANE Select ENSP00000417980.1:n.1502-217_1502-216delinsAG
ENST00000629335.2:c.1502-217_1502-216delinsAG ENSP00000490056.1:n.1502-217_1502-216delinsAG
ENST00000636027.1:c.1388-217_1388-216delinsAG ENSP00000489961.1:n.1388-217_1388-216delinsAG
ENST00000637161.1:c.1409-217_1409-216delinsAG ENSP00000490328.1:n.1409-217_1409-216delinsAG
ENST00000637261.1:c.1542-217_1542-216delinsAG ENSP00000490815.1:n.1542-217_1542-216delinsAG
ENST00000637977.1:c.1447-217_1447-216delinsAG
ENST00000638071.1:c.1129-217_1129-216delinsAG
ENST00000640639.1:c.671-217_671-216delinsAG ENSP00000491823.1:n.671-217_671-216delinsAG
ENST00000371394.6:c.*1237-217_*1237-216delinsAG ENSP00000485945.1:n.*1237-217_*1237-216delinsAG
ENST00000460843.5:c.1502-217_1502-216delinsAG ENSP00000417980.1:n.1502-217_1502-216delinsAG
ENST00000462484.5:c.1502-217_1502-216delinsAG ENSP00000417328.1:n.1502-217_1502-216delinsAG
ENST00000462942.3:c.359-217_359-216delinsAG ENSP00000436107.1:n.359-217_359-216delinsAG
ENST00000465566.2:c.194-217_194-216delinsAG ENSP00000486261.1:n.194-217_194-216delinsAG
ENST00000629808.2:c.595-217_595-216delinsAG
NM_001145527.1:c.1502-217_1502-216delinsAG NP_001138999.1:n.1502-217_1502-216delinsAG
NM_024757.4:c.1502-217_1502-216delinsAG NP_079033.4:n.1502-217_1502-216delinsAG
XM_005266105.3:c.1493-217_1493-216delinsAG XP_005266162.1:n.1493-217_1493-216delinsAG
XM_005266110.1:c.1409-217_1409-216delinsAG XP_005266167.1:n.1409-217_1409-216delinsAG
XM_006717288.2:c.1484-217_1484-216delinsAG XP_006717351.1:n.1484-217_1484-216delinsAG
XM_011519021.1:c.1511-217_1511-216delinsAG XP_011517323.1:n.1511-217_1511-216delinsAG
XM_011519022.1:c.1508-217_1508-216delinsAG XP_011517324.1:n.1508-217_1508-216delinsAG
XM_011519023.1:c.1490-217_1490-216delinsAG XP_011517325.1:n.1490-217_1490-216delinsAG
XM_011519024.1:c.1433-217_1433-216delinsAG XP_011517326.1:n.1433-217_1433-216delinsAG
XM_011519025.1:c.1409-217_1409-216delinsAG XP_011517327.1:n.1409-217_1409-216delinsAG
XM_011519026.1:c.1511-217_1511-216delinsAG XP_011517328.1:n.1511-217_1511-216delinsAG
XM_011519027.1:c.1511-217_1511-216delinsAG XP_011517329.1:n.1511-217_1511-216delinsAG
XM_011519028.1:c.1511-217_1511-216delinsAG XP_011517330.1:n.1511-217_1511-216delinsAG
XM_011519029.1:c.-68-217_-68-216delinsAG XP_011517331.1:n.-68-217_-68-216delinsAG
XM_011519033.1:c.1490-217_1490-216delinsAG XP_011517335.1:n.1490-217_1490-216delinsAG
NM_001354259.1:c.1409-217_1409-216delinsAG NP_001341188.1:n.1409-217_1409-216delinsAG
NM_001354263.1:c.1481-217_1481-216delinsAG NP_001341192.1:n.1481-217_1481-216delinsAG
NM_001354611.1:c.1502-217_1502-216delinsAG NP_001341540.1:n.1502-217_1502-216delinsAG
NM_001354612.1:c.1409-217_1409-216delinsAG NP_001341541.1:n.1409-217_1409-216delinsAG
XM_005266105.5:c.1493-217_1493-216delinsAG XP_005266162.1:n.1493-217_1493-216delinsAG
XM_011519021.3:c.1511-217_1511-216delinsAG XP_011517323.1:n.1511-217_1511-216delinsAG
XM_011519022.3:c.1508-217_1508-216delinsAG XP_011517324.1:n.1508-217_1508-216delinsAG
XM_011519023.3:c.1490-217_1490-216delinsAG XP_011517325.1:n.1490-217_1490-216delinsAG
XM_011519029.3:c.-68-217_-68-216delinsAG XP_011517331.1:n.-68-217_-68-216delinsAG
XM_017015134.1:c.1487-217_1487-216delinsAG XP_016870623.1:n.1487-217_1487-216delinsAG
XM_017015136.2:c.1403-217_1403-216delinsAG XP_016870625.1:n.1403-217_1403-216delinsAG
XM_017015137.1:c.1388-217_1388-216delinsAG XP_016870626.1:n.1388-217_1388-216delinsAG
XM_017015138.1:c.1388-217_1388-216delinsAG XP_016870627.1:n.1388-217_1388-216delinsAG
XM_024447674.1:c.1331-217_1331-216delinsAG XP_024303442.1:n.1331-217_1331-216delinsAG
XM_024447675.1:c.1409-217_1409-216delinsAG XP_024303443.1:n.1409-217_1409-216delinsAG
XM_024447676.1:c.626-217_626-216delinsAG XP_024303444.1:n.626-217_626-216delinsAG
XM_024447677.1:c.626-217_626-216delinsAG XP_024303445.1:n.626-217_626-216delinsAG
XM_024447678.1:c.1409-217_1409-216delinsAG XP_024303446.1:n.1409-217_1409-216delinsAG
XM_024447679.1:c.1409-217_1409-216delinsAG XP_024303447.1:n.1409-217_1409-216delinsAG
XM_024447680.1:c.1388-217_1388-216delinsAG XP_024303448.1:n.1388-217_1388-216delinsAG
NM_024757.5:c.1502-217_1502-216delinsAG MANE Select NP_079033.4:n.1502-217_1502-216delinsAG
NM_001145527.2:c.1502-217_1502-216delinsAG NP_001138999.1:n.1502-217_1502-216delinsAG
NM_001354259.2:c.1409-217_1409-216delinsAG NP_001341188.1:n.1409-217_1409-216delinsAG
NM_001354263.2:c.1481-217_1481-216delinsAG NP_001341192.1:n.1481-217_1481-216delinsAG
NM_001354611.2:c.1502-217_1502-216delinsAG NP_001341540.1:n.1502-217_1502-216delinsAG
NM_001354612.2:c.1409-217_1409-216delinsAG NP_001341541.1:n.1409-217_1409-216delinsAG
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