HGVS | Genome Assembly |
---|---|
NC_000009.12:g.136687185_136687187del , CM000671.2:g.136687185_136687187del | GRCh38 |
NC_000009.11:g.139581637_139581639del , CM000671.1:g.139581637_139581639del | GRCh37 |
NC_000009.10:g.138701458_138701460del | NCBI36 |
NG_008090.1:g.5274_5276del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371696.7:c.172_174del MANE Select | ENSP00000360761.2:p.Glu58del | |
ENST00000371694.7:c.172_174del | ENSP00000360759.3:p.Glu58del | |
ENST00000371696.6:c.172_174del | ENSP00000360761.2:p.Glu58del | |
ENST00000470861.1:n.180_182del | ||
ENST00000538402.1:c.172_174del | ENSP00000438919.1:p.Glu58del | |
NM_001012727.1:c.172_174del | NP_001012745.1:p.Glu58del | |
NM_006412.3:c.172_174del | NP_006403.2:p.Glu58del | |
NM_006412.4:c.172_174del MANE Select | NP_006403.2:p.Glu58del | |
NM_001012727.2:c.172_174del | NP_001012745.1:p.Glu58del |