HGVS | Genome Assembly |
---|---|
NC_000011.10:g.64746983del , CM000673.2:g.64746983del | GRCh38 |
NC_000011.9:g.64514455del , CM000673.1:g.64514455del | GRCh37 |
NC_000011.8:g.64271031del | NCBI36 |
NG_007574.1:g.3476del , LRG_100:g.3476del | |
NG_013018.1:g.18735del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000164139.4:c.2319del MANE Select | ENSP00000164139.3:p.Val774SerfsTer29 | |
ENST00000164139.3:c.2319del | ENSP00000164139.3:p.Val774SerfsTer29 | |
ENST00000377432.7:c.2055del | ENSP00000366650.3:p.Val686SerfsTer29 | |
ENST00000483742.1:n.1672del | ||
NM_001164716.1:c.2055del | NP_001158188.1:p.Val686SerfsTer29 | |
NM_005609.2:c.2319del | NP_005600.1:p.Val774SerfsTer29 | |
NM_005609.3:c.2319del | NP_005600.1:p.Val774SerfsTer29 | |
NM_005609.4:c.2319del MANE Select | NP_005600.1:p.Val774SerfsTer29 |