HGVS | Genome Assembly |
---|---|
NC_000007.14:g.17339708del , CM000669.2:g.17339708del | GRCh38 |
NC_000007.13:g.17379332del , CM000669.1:g.17379332del | GRCh37 |
NC_000007.12:g.17345857del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242057.9:c.1883del MANE Select | ENSP00000242057.4:p.Lys628SerfsTer3 | |
ENST00000637807.1:c.1853del | ENSP00000490530.1:p.Lys618SerfsTer3 | |
ENST00000642825.1:c.1838del | ENSP00000495987.1:p.Lys613SerfsTer3 | |
ENST00000242057.8:c.1883del | ENSP00000242057.4:p.Lys628SerfsTer3 | |
ENST00000463496.1:c.1883del | ENSP00000436466.1:p.Lys628SerfsTer3 | |
NM_001621.4:c.1883del | NP_001612.1:p.Lys628SerfsTer3 | |
NM_001621.5:c.1883del MANE Select | NP_001612.1:p.Lys628SerfsTer3 |