HGVS | Genome Assembly |
---|---|
NC_000017.11:g.8076447del , CM000679.2:g.8076447del | GRCh38 |
NC_000017.10:g.7979765del , CM000679.1:g.7979765del | GRCh37 |
NC_000017.9:g.7920490del | NCBI36 |
NG_007099.1:g.16259del | |
NG_007099.2:g.16272del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647874.1:c.1363-101del MANE Select | ENSP00000497784.1:n.1363-101del | |
ENST00000649809.1:c.427-101del | ENSP00000496845.1:n.427-101del | |
ENST00000319144.4:c.1363-101del | ENSP00000315167.4:n.1363-101del | |
ENST00000577351.5:n.310-101del | ||
ENST00000583276.5:n.747-101del | ||
ENST00000584116.1:n.619-101del | ||
NM_001139.2:c.1363-101del | NP_001130.1:n.1363-101del | |
NM_001139.3:c.1363-101del MANE Select | NP_001130.1:n.1363-101del |