Canonical Allele Identifier: CA2636448665
Gene: MYO15A HGNC NCBI

Linked Data

gnomAD v4: 17-18146089-TCAA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146093_18146095del , CM000679.2:g.18146093_18146095del GRCh38
NC_000017.10:g.18049407_18049409del , CM000679.1:g.18049407_18049409del GRCh37
NC_000017.9:g.17990132_17990134del NCBI36
NG_011634.1:g.42388_42390del
NG_011634.2:g.42388_42390del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6495_6497del MANE Select ENSP00000495481.1:p.Asn2165del
ENST00000205890.9:c.6495_6497del ENSP00000205890.5:p.Asn2165del
ENST00000578999.1:n.80_82del
ENST00000615845.4:c.6495_6497del ENSP00000481642.1:p.Asn2165del
NM_016239.3:c.6495_6497del NP_057323.3:p.Asn2165del
XM_011523917.1:c.6435_6437del XP_011522219.1:p.Asn2145del
XM_011523918.1:c.6342+93_6342+95del XP_011522220.1:n.6342+93_6342+95del
XM_011523921.1:c.6489_6491del XP_011522223.1:p.Asn2163del
XR_934037.1:n.7094_7096del
XR_934038.1:n.7094_7096del
XM_011523918.2:c.6342+93_6342+95del XP_011522220.1:n.6342+93_6342+95del
XM_017024714.2:c.6435_6437del XP_016880203.1:p.Asn2145del
XM_017024715.2:c.6498_6500del XP_016880204.1:p.Asn2166del
XM_024450781.1:c.6213+1501_6213+1503del XP_024306549.1:n.6213+1501_6213+1503del
NM_016239.4:c.6495_6497del MANE Select NP_057323.3:p.Asn2165del
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