Canonical Allele Identifier: CA398607398
Gene: MYO15A HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.18049403T>A (hg19) chr17:g.18146089T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146089T>A , CM000679.2:g.18146089T>A GRCh38
NC_000017.10:g.18049403T>A , CM000679.1:g.18049403T>A GRCh37
NC_000017.9:g.17990128T>A NCBI36
NG_011634.1:g.42384T>A
NG_011634.2:g.42384T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6491T>A MANE Select ENSP00000495481.1:p.Phe2164Tyr
ENST00000205890.9:c.6491T>A ENSP00000205890.5:p.Phe2164Tyr
ENST00000578999.1:n.76T>A
ENST00000615845.4:c.6491T>A ENSP00000481642.1:p.Phe2164Tyr
NM_016239.3:c.6491T>A NP_057323.3:p.Phe2164Tyr
XM_011523917.1:c.6431T>A XP_011522219.1:p.Phe2144Tyr
XM_011523918.1:c.6342+89T>A XP_011522220.1:n.6342+89T>A
XM_011523921.1:c.6485T>A XP_011522223.1:p.Phe2162Tyr
XR_934037.1:n.7090T>A
XR_934038.1:n.7090T>A
XM_011523918.2:c.6342+89T>A XP_011522220.1:n.6342+89T>A
XM_017024714.2:c.6431T>A XP_016880203.1:p.Phe2144Tyr
XM_017024715.2:c.6494T>A XP_016880204.1:p.Phe2165Tyr
XM_024450781.1:c.6213+1497T>A XP_024306549.1:n.6213+1497T>A
NM_016239.4:c.6491T>A MANE Select NP_057323.3:p.Phe2164Tyr
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