HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152648411_152648413delinsAAG , CM000669.2:g.152648411_152648413delinsAAG | GRCh38 |
NC_000007.13:g.152345496_152345498delinsAAG , CM000669.1:g.152345496_152345498delinsAAG | GRCh37 |
NC_000007.12:g.151976429_151976431delinsAAG | NCBI36 |
NG_027988.1:g.32753_32755delinsCTT | |
NG_027988.2:g.32753_32755delinsCTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698506.1:c.*229_*231delinsCTT | ENSP00000513758.1:n.*229_*231delinsCTT | |
ENST00000359321.2:c.*229_*231delinsCTT MANE Select | ENSP00000352271.1:n.*229_*231delinsCTT | |
ENST00000359321.1:c.*229_*231delinsCTT | ENSP00000352271.1:n.*229_*231delinsCTT | |
ENST00000495707.1:n.1094_1096delinsCTT | ||
NM_005431.1:c.*229_*231delinsCTT | NP_005422.1:n.*229_*231delinsCTT | |
NM_005431.2:c.*229_*231delinsCTT MANE Select | NP_005422.1:n.*229_*231delinsCTT |