Canonical Allele Identifier: CA2808664867
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145949del , CM000679.2:g.18145949del GRCh38
NC_000017.10:g.18049263del , CM000679.1:g.18049263del GRCh37
NC_000017.9:g.17989988del NCBI36
NG_011634.1:g.42244del
NG_011634.2:g.42244del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6351del MANE Select ENSP00000495481.1:p.Leu2118TrpfsTer?
ENST00000205890.9:c.6351del ENSP00000205890.5:p.Leu2118TrpfsTer?
ENST00000615845.4:c.6351del ENSP00000481642.1:p.Leu2118TrpfsTer?
NM_016239.3:c.6351del NP_057323.3:p.Leu2118TrpfsTer?
XM_011523917.1:c.6291del XP_011522219.1:p.Leu2098TrpfsTer?
XM_011523918.1:c.6291del XP_011522220.1:p.Leu2098TrpfsTer?
XM_011523921.1:c.6345del XP_011522223.1:p.Leu2116TrpfsTer?
XR_934037.1:n.6950del
XR_934038.1:n.6950del
XM_011523918.2:c.6291del XP_011522220.1:p.Leu2098TrpfsTer?
XM_017024714.2:c.6291del XP_016880203.1:p.Leu2098TrpfsTer?
XM_017024715.2:c.6354del XP_016880204.1:p.Leu2119TrpfsTer?
XM_024450781.1:c.6213+1357del XP_024306549.1:n.6213+1357del
NM_016239.4:c.6351del MANE Select NP_057323.3:p.Leu2118TrpfsTer?