HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152648412_152648413delinsAG , CM000669.2:g.152648412_152648413delinsAG | GRCh38 |
NC_000007.13:g.152345497_152345498delinsAG , CM000669.1:g.152345497_152345498delinsAG | GRCh37 |
NC_000007.12:g.151976430_151976431delinsAG | NCBI36 |
NG_027988.1:g.32753_32754delinsCT | |
NG_027988.2:g.32753_32754delinsCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698506.1:c.*229_*230delinsCT | ENSP00000513758.1:n.*229_*230delinsCT | |
ENST00000359321.2:c.*229_*230delinsCT MANE Select | ENSP00000352271.1:n.*229_*230delinsCT | |
ENST00000359321.1:c.*229_*230delinsCT | ENSP00000352271.1:n.*229_*230delinsCT | |
ENST00000495707.1:n.1094_1095delinsCT | ||
NM_005431.1:c.*229_*230delinsCT | NP_005422.1:n.*229_*230delinsCT | |
NM_005431.2:c.*229_*230delinsCT MANE Select | NP_005422.1:n.*229_*230delinsCT |