HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52028025_52028026insTT , CM000666.2:g.52028025_52028026insTT | GRCh38 |
NC_000004.11:g.52894191_52894192insTT , CM000666.1:g.52894191_52894192insTT | GRCh37 |
NC_000004.10:g.52588948_52588949insTT | NCBI36 |
NG_008891.1:g.15295_15296insAA , LRG_204:g.15295_15296insAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.696_697insAA MANE Select | ENSP00000370839.6:p.Phe233AsnfsTer18 | |
ENST00000381431.9:c.696_697insAA | ENSP00000370839.5:p.Phe233AsnfsTer18 | |
NM_000232.4:c.696_697insAA , LRG_204t1:c.696_697insAA | NP_000223.1:p.Phe233AsnfsTer18 | |
XM_006714049.2:c.399_400insAA | XP_006714112.1:p.Phe134AsnfsTer18 | |
XM_011534403.1:c.486_487insAA | XP_011532705.1:p.Phe163AsnfsTer18 | |
XM_011534404.1:c.399_400insAA | XP_011532706.1:p.Phe134AsnfsTer18 | |
NM_000232.5:c.696_697insAA MANE Select | NP_000223.1:p.Phe233AsnfsTer18 |