HGVS | Genome Assembly |
---|---|
NC_000007.14:g.95318620_95318621delinsAT , CM000669.2:g.95318620_95318621delinsAT | GRCh38 |
NC_000007.13:g.94947932_94947933delinsAT , CM000669.1:g.94947932_94947933delinsAT | GRCh37 |
NC_000007.12:g.94785868_94785869delinsAT | NCBI36 |
NG_008779.1:g.10952_10953delinsAT | |
NG_008779.2:g.11086_11087delinsAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222381.8:c.75-228_75-227delinsAT MANE Select | ENSP00000222381.3:n.75-228_75-227delinsAT | |
ENST00000222381.7:c.75-228_75-227delinsAT | ENSP00000222381.3:n.75-228_75-227delinsAT | |
ENST00000433729.1:c.75-228_75-227delinsAT | ENSP00000407359.1:n.75-228_75-227delinsAT | |
NM_000446.5:c.75-228_75-227delinsAT | NP_000437.3:n.75-228_75-227delinsAT | |
NM_000446.6:c.75-228_75-227delinsAT | NP_000437.3:n.75-228_75-227delinsAT | |
NM_000446.7:c.75-228_75-227delinsAT MANE Select | NP_000437.3:n.75-228_75-227delinsAT |