HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21854348_21854350del , CM000669.2:g.21854348_21854350del | GRCh38 |
NC_000007.13:g.21893966_21893968del , CM000669.1:g.21893966_21893968del | GRCh37 |
NC_000007.12:g.21860491_21860493del | NCBI36 |
NG_012886.2:g.316134_316136del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409508.8:c.11095_11097del MANE Select | ENSP00000475939.1:p.Asn3699del | |
ENST00000328843.10:c.11116_11118del | ENSP00000330671.7:p.Asn3706del | |
ENST00000409508.7:c.11095_11097del | ENSP00000475939.1:p.Asn3699del | |
ENST00000421290.1:n.278_280del | ||
ENST00000607413.5:n.358_360del | ||
ENST00000620169.4:c.11116_11118del | ENSP00000481693.1:p.Asn3706del | |
NM_001277115.1:c.11095_11097del | NP_001264044.1:p.Asn3699del | |
NM_001277115.2:c.11095_11097del MANE Select | NP_001264044.1:p.Asn3699del |