HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110602222del , CM000672.2:g.110602222del | GRCh38 |
NC_000010.10:g.112361980del , CM000672.1:g.112361980del | GRCh37 |
NC_000010.9:g.112351970del | NCBI36 |
NG_012217.1:g.39532del , LRG_774:g.39532del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.5338+44del | ||
ENST00000685743.1:n.2813+44del | ||
ENST00000686057.1:n.1456+44del | ||
ENST00000689321.1:n.2068+44del | ||
ENST00000689986.1:n.894+44del | ||
ENST00000361804.5:c.3105+44del MANE Select | ENSP00000354720.5:n.3105+44del | |
ENST00000361804.4:c.3105+44del | ENSP00000354720.4:n.3105+44del | |
NM_005445.3:c.3105+44del , LRG_774t1:c.3105+44del | NP_005436.1:n.3105+44del | |
NM_005445.4:c.3105+44del MANE Select | NP_005436.1:n.3105+44del |