Canonical Allele Identifier: CA2576190685
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18150375del , CM000679.2:g.18150375del GRCh38
NC_000017.10:g.18053689del , CM000679.1:g.18053689del GRCh37
NC_000017.9:g.17994414del NCBI36
NG_011634.1:g.46670del
NG_011634.2:g.46670del

Transcript Alleles

HGVS Amino-acid change
ENST00000647165.2:c.7213-54del MANE Select ENSP00000495481.1:n.7213-54del
ENST00000205890.9:c.7213-54del ENSP00000205890.5:n.7213-54del
ENST00000615845.4:c.7213-54del ENSP00000481642.1:n.7213-54del
NM_016239.3:c.7213-54del NP_057323.3:n.7213-54del
XM_011523917.1:c.6888-54del XP_011522219.1:n.6888-54del
XM_011523921.1:c.7207-54del XP_011522223.1:n.7207-54del
XR_934037.1:n.7547-54del
XR_934038.1:n.7499-54del
XR_934293.1:n.434+1229del
XR_934294.1:n.435-601del
XR_934295.1:n.253+1229del
XM_017024714.2:c.7153-54del XP_016880203.1:n.7153-54del
XM_017024715.2:c.7216-54del XP_016880204.1:n.7216-54del
XR_934293.2:n.377+1229del
XR_934294.2:n.378-601del
NM_016239.4:c.7213-54del MANE Select NP_057323.3:n.7213-54del