Canonical Allele Identifier: CA2692895023
Gene: EHMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137818267del , CM000671.2:g.137818267del GRCh38
NC_000009.11:g.140712719del , CM000671.1:g.140712719del GRCh37
NC_000009.10:g.139832540del NCBI36
NG_011776.1:g.204276del

Transcript Alleles

HGVS Amino-acid Change
ENST00000460843.6:c.3540+129del MANE Select ENSP00000417980.1:n.3540+129del
ENST00000636526.1:n.26+129del
ENST00000637161.1:c.3447+129del ENSP00000490328.1:n.3447+129del
ENST00000637261.1:c.4114+129del ENSP00000490815.1:n.4114+129del
ENST00000637748.1:n.521+129del
ENST00000637891.1:c.1614+129del ENSP00000490907.1:n.1614+129del
ENST00000460843.5:c.3540+129del ENSP00000417980.1:n.3540+129del
ENST00000462942.3:c.2397+129del ENSP00000436107.1:n.2397+129del
ENST00000475564.5:n.1264+129del
ENST00000494249.5:n.893+129del
NM_024757.4:c.3540+129del NP_079033.4:n.3540+129del
XM_005266105.3:c.3531+129del XP_005266162.1:n.3531+129del
XM_005266110.1:c.3447+129del XP_005266167.1:n.3447+129del
XM_006717288.2:c.3522+129del XP_006717351.1:n.3522+129del
XM_011519021.1:c.3549+129del XP_011517323.1:n.3549+129del
XM_011519022.1:c.3546+129del XP_011517324.1:n.3546+129del
XM_011519023.1:c.3528+129del XP_011517325.1:n.3528+129del
XM_011519024.1:c.3471+129del XP_011517326.1:n.3471+129del
XM_011519025.1:c.3447+129del XP_011517327.1:n.3447+129del
XM_011519026.1:c.3405+129del XP_011517328.1:n.3405+129del
XM_011519029.1:c.1971+129del XP_011517331.1:n.1971+129del
XM_011519030.1:c.1323+129del XP_011517332.1:n.1323+129del
XM_011519031.1:c.1110+129del XP_011517333.1:n.1110+129del
XM_011519032.1:c.1110+129del XP_011517334.1:n.1110+129del
XM_011519033.1:c.3384+129del XP_011517335.1:n.3384+129del
XR_930459.1:n.5297-3704del
NM_001354263.1:c.3519+129del NP_001341192.1:n.3519+129del
XM_005266105.5:c.3531+129del XP_005266162.1:n.3531+129del
XM_011519021.3:c.3549+129del XP_011517323.1:n.3549+129del
XM_011519022.3:c.3546+129del XP_011517324.1:n.3546+129del
XM_011519023.3:c.3528+129del XP_011517325.1:n.3528+129del
XM_011519029.3:c.1971+129del XP_011517331.1:n.1971+129del
XM_011519030.3:c.1323+129del XP_011517332.1:n.1323+129del
XM_017015134.1:c.3525+129del XP_016870623.1:n.3525+129del
XM_017015136.2:c.3441+129del XP_016870625.1:n.3441+129del
XM_017015137.1:c.3426+129del XP_016870626.1:n.3426+129del
XM_017015138.1:c.3426+129del XP_016870627.1:n.3426+129del
XM_024447674.1:c.3369+129del XP_024303442.1:n.3369+129del
XM_024447675.1:c.3303+129del XP_024303443.1:n.3303+129del
XM_024447676.1:c.2664+129del XP_024303444.1:n.2664+129del
XM_024447677.1:c.2664+129del XP_024303445.1:n.2664+129del
XM_024447680.1:c.3282+129del XP_024303448.1:n.3282+129del
NM_024757.5:c.3540+129del MANE Select NP_079033.4:n.3540+129del
NM_001354263.2:c.3519+129del NP_001341192.1:n.3519+129del