HGVS | Genome Assembly |
---|---|
NC_000005.10:g.178994841_178994858del , CM000667.2:g.178994841_178994858del | GRCh38 |
NC_000005.9:g.178421842_178421859del , CM000667.1:g.178421842_178421859del | GRCh37 |
NC_000005.8:g.178354448_178354465del | NCBI36 |
NG_008105.1:g.5273_5290del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000517717.3:c.94_111del MANE Select | ENSP00000430767.1:p.Ser32_Gly37del | |
ENST00000650031.1:c.94_111del | ENSP00000497110.1:p.Ser32_Gly37del | |
ENST00000231188.9:c.94_111del | ENSP00000231188.5:p.Ser32_Gly37del | |
ENST00000517717.1:c.94_111del | ENSP00000430767.1:p.Ser32_Gly37del | |
NM_000843.3:c.94_111del | NP_000834.2:p.Ser32_Gly37del | |
NM_000843.4:c.94_111del MANE Select | NP_000834.2:p.Ser32_Gly37del |