Canonical Allele Identifier: CA2573054345
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18135826_18135827del , CM000679.2:g.18135826_18135827del GRCh38
NC_000017.10:g.18039140_18039141del , CM000679.1:g.18039140_18039141del GRCh37
NC_000017.9:g.17979865_17979866del NCBI36
NG_011634.1:g.32121_32122del
NG_011634.2:g.32121_32122del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.4596+2_4596+3del MANE Select ENSP00000495481.1:n.4596+2_4596+3del
ENST00000205890.9:c.4596+2_4596+3del ENSP00000205890.5:n.4596+2_4596+3del
ENST00000615845.4:c.4596+2_4596+3del ENSP00000481642.1:n.4596+2_4596+3del
NM_016239.3:c.4596+2_4596+3del NP_057323.3:n.4596+2_4596+3del
XM_011523917.1:c.4590+2_4590+3del XP_011522219.1:n.4590+2_4590+3del
XM_011523918.1:c.4590+2_4590+3del XP_011522220.1:n.4590+2_4590+3del
XM_011523919.1:c.4590+2_4590+3del XP_011522221.1:n.4590+2_4590+3del
XM_011523920.1:c.4590+2_4590+3del XP_011522222.1:n.4590+2_4590+3del
XM_011523921.1:c.4590+2_4590+3del XP_011522223.1:n.4590+2_4590+3del
XR_934037.1:n.5249+2_5249+3del
XR_934038.1:n.5249+2_5249+3del
XR_934039.1:n.5249+2_5249+3del
XM_011523918.2:c.4590+2_4590+3del XP_011522220.1:n.4590+2_4590+3del
XM_017024714.2:c.4590+2_4590+3del XP_016880203.1:n.4590+2_4590+3del
XM_017024715.2:c.4599+2_4599+3del XP_016880204.1:n.4599+2_4599+3del
XM_024450780.1:c.4590+2_4590+3del XP_024306548.1:n.4590+2_4590+3del
XM_024450781.1:c.4590+2_4590+3del XP_024306549.1:n.4590+2_4590+3del
XM_024450782.1:c.4590+2_4590+3del XP_024306550.1:n.4590+2_4590+3del
XR_934039.2:n.5288+2_5288+3del
NM_016239.4:c.4596+2_4596+3del MANE Select NP_057323.3:n.4596+2_4596+3del