HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110602027del , CM000672.2:g.110602027del | GRCh38 |
NC_000010.10:g.112361785del , CM000672.1:g.112361785del | GRCh37 |
NC_000010.9:g.112351775del | NCBI36 |
NG_012217.1:g.39337del , LRG_774:g.39337del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.5187del | ||
ENST00000685743.1:n.2662del | ||
ENST00000686057.1:n.1305del | ||
ENST00000689321.1:n.1917del | ||
ENST00000689986.1:n.743del | ||
ENST00000361804.5:c.2954del MANE Select | ENSP00000354720.5:p.Lys985ArgfsTer7 | |
ENST00000361804.4:c.2954del | ENSP00000354720.4:p.Lys985ArgfsTer7 | |
NM_005445.3:c.2954del , LRG_774t1:c.2954del | NP_005436.1:p.Lys985ArgfsTer7 | |
NM_005445.4:c.2954del MANE Select | NP_005436.1:p.Lys985ArgfsTer7 |