HGVS | Genome Assembly |
---|---|
NC_000009.12:g.136687387_136687388del , CM000671.2:g.136687387_136687388del | GRCh38 |
NC_000009.11:g.139581839_139581840del , CM000671.1:g.139581839_139581840del | GRCh37 |
NC_000009.10:g.138701660_138701661del | NCBI36 |
NG_008090.1:g.5072_5073del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371696.7:c.-31_-30del MANE Select | ENSP00000360761.2:n.-31_-30del | |
ENST00000371694.7:c.-31_-30del | ENSP00000360759.3:n.-31_-30del | |
ENST00000371696.6:c.-31_-30del | ENSP00000360761.2:n.-31_-30del | |
ENST00000538402.1:c.-31_-30del | ENSP00000438919.1:n.-31_-30del | |
NM_001012727.1:c.-31_-30del | NP_001012745.1:n.-31_-30del | |
NM_006412.3:c.-31_-30del | NP_006403.2:n.-31_-30del | |
NM_006412.4:c.-31_-30del MANE Select | NP_006403.2:n.-31_-30del | |
NM_001012727.2:c.-31_-30del | NP_001012745.1:n.-31_-30del |