HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152675664_152675665delinsAG , CM000669.2:g.152675664_152675665delinsAG | GRCh38 |
NC_000007.13:g.152372749_152372750delinsAG , CM000669.1:g.152372749_152372750delinsAG | GRCh37 |
NC_000007.12:g.152003682_152003683delinsAG | NCBI36 |
NG_027988.1:g.5501_5502delinsCT | |
NG_027988.2:g.5501_5502delinsCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698506.1:c.-48+376_-48+377delinsCT | ENSP00000513758.1:n.-48+376_-48+377delinsCT | |
ENST00000698507.1:n.107+376_107+377delinsCT | ||
ENST00000359321.2:c.39+376_39+377delinsCT MANE Select | ENSP00000352271.1:n.39+376_39+377delinsCT | |
ENST00000359321.1:c.39+376_39+377delinsCT | ENSP00000352271.1:n.39+376_39+377delinsCT | |
NM_005431.1:c.39+376_39+377delinsCT | NP_005422.1:n.39+376_39+377delinsCT | |
NM_005431.2:c.39+376_39+377delinsCT MANE Select | NP_005422.1:n.39+376_39+377delinsCT |