HGVS | Genome Assembly |
---|---|
NC_000007.14:g.1234101_1234103delinsCAA , CM000669.2:g.1234101_1234103delinsCAA | GRCh38 |
NC_000007.13:g.1273737_1273739delinsCAA , CM000669.1:g.1273737_1273739delinsCAA | GRCh37 |
NC_000007.12:g.1240263_1240265delinsCAA | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000316333.9:c.450+406_450+408delinsCAA MANE Select | ENSP00000314480.8:n.450+406_450+408delins... | |
ENST00000316333.8:c.450+406_450+408delinsCAA | ENSP00000314480.8:n.450+406_450+408delins... | |
NM_001080461.1:c.450+406_450+408delinsCAA | NP_001073930.1:n.450+406_450+408delinsCAA... | |
NM_001080461.2:c.450+406_450+408delinsCAA | NP_001073930.1:n.450+406_450+408delinsCAA... | |
NM_001080461.3:c.450+406_450+408delinsCAA MANE Select | NP_001073930.1:n.450+406_450+408delinsCAA... |