Canonical Allele Identifier: CA2697559470
Gene: MYO15A HGNC NCBI

Linked Data

ClinVar Variation Id: 2697721
ClinVar RCV Id: RCV003549424
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146128del , CM000679.2:g.18146128del GRCh38
NC_000017.10:g.18049442del , CM000679.1:g.18049442del GRCh37
NC_000017.9:g.17990167del NCBI36
NG_011634.1:g.42423del
NG_011634.2:g.42423del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6509+21del MANE Select ENSP00000495481.1:n.6509+21del
ENST00000205890.9:c.6509+21del ENSP00000205890.5:n.6509+21del
ENST00000578999.1:n.94+21del
ENST00000615845.4:c.6509+21del ENSP00000481642.1:n.6509+21del
NM_016239.3:c.6509+21del NP_057323.3:n.6509+21del
XM_011523917.1:c.6449+21del XP_011522219.1:n.6449+21del
XM_011523918.1:c.6342+128del XP_011522220.1:n.6342+128del
XM_011523921.1:c.6503+21del XP_011522223.1:n.6503+21del
XR_934037.1:n.7108+21del
XR_934038.1:n.7108+21del
XM_011523918.2:c.6342+128del XP_011522220.1:n.6342+128del
XM_017024714.2:c.6449+21del XP_016880203.1:n.6449+21del
XM_017024715.2:c.6512+21del XP_016880204.1:n.6512+21del
XM_024450781.1:c.6213+1536del XP_024306549.1:n.6213+1536del
NM_016239.4:c.6509+21del MANE Select NP_057323.3:n.6509+21del
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