HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128840997del , CM000669.2:g.128840997del | GRCh38 |
NC_000007.13:g.128481051del , CM000669.1:g.128481051del | GRCh37 |
NC_000007.12:g.128268287del | NCBI36 |
NG_011807.1:g.15569del , LRG_870:g.15569del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325888.13:c.1813+27del MANE Select | ENSP00000327145.8:n.1813+27del | |
ENST00000325888.12:c.1813+27del | ENSP00000327145.8:n.1813+27del | |
ENST00000346177.6:c.1813+27del | ENSP00000344002.6:n.1813+27del | |
NM_001127487.1:c.1813+27del | NP_001120959.1:n.1813+27del | |
NM_001458.4:c.1813+27del , LRG_870t1:c.1813+27del | NP_001449.3:n.1813+27del | |
NM_001127487.2:c.1813+27del | NP_001120959.1:n.1813+27del | |
NM_001458.5:c.1813+27del MANE Select | NP_001449.3:n.1813+27del |