HGVS | Genome Assembly |
---|---|
NC_000007.14:g.147132375del , CM000669.2:g.147132375del | GRCh38 |
NC_000007.13:g.146829467del , CM000669.1:g.146829467del | GRCh37 |
NC_000007.12:g.146460400del | NCBI36 |
NG_007092.2:g.1021015del | |
NG_007092.3:g.1021375del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361727.8:c.1214del MANE Select | ENSP00000354778.3:p.Asn405ThrfsTer? | |
ENST00000636561.1:n.1117del | ||
ENST00000636870.1:n.1076del | ||
ENST00000637150.1:n.1143del | ||
ENST00000637694.1:n.1117del | ||
ENST00000637825.1:n.697del | ||
ENST00000638117.1:n.1117del | ||
ENST00000361727.7:c.1214del | ENSP00000354778.3:p.Asn405ThrfsTer? | |
NM_014141.5:c.1214del | NP_054860.1:p.Asn405ThrfsTer? | |
XM_017011950.2:c.1214del | XP_016867439.1:p.Asn405ThrfsTer? | |
NM_014141.6:c.1214del MANE Select | NP_054860.1:p.Asn405ThrfsTer? |