HGVS | Genome Assembly |
---|---|
NC_000009.12:g.136674009del , CM000671.2:g.136674009del | GRCh38 |
NC_000009.11:g.139568461del , CM000671.1:g.139568461del | GRCh37 |
NC_000009.10:g.138688282del | NCBI36 |
NG_008090.1:g.18454del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371696.7:c.662-79del MANE Select | ENSP00000360761.2:n.662-79del | |
ENST00000371694.7:c.566-79del | ENSP00000360759.3:n.566-79del | |
ENST00000371696.6:c.662-79del | ENSP00000360761.2:n.662-79del | |
ENST00000472820.1:n.590-79del | ||
ENST00000538402.1:c.662-79del | ENSP00000438919.1:n.662-79del | |
NM_001012727.1:c.566-79del | NP_001012745.1:n.566-79del | |
NM_006412.3:c.662-79del | NP_006403.2:n.662-79del | |
NM_006412.4:c.662-79del MANE Select | NP_006403.2:n.662-79del | |
NM_001012727.2:c.566-79del | NP_001012745.1:n.566-79del |