Canonical Allele Identifier: CA398606520
Gene: MYO15A HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.18049238T>A (hg19) chr17:g.18145924T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145924T>A , CM000679.2:g.18145924T>A GRCh38
NC_000017.10:g.18049238T>A , CM000679.1:g.18049238T>A GRCh37
NC_000017.9:g.17989963T>A NCBI36
NG_011634.1:g.42219T>A
NG_011634.2:g.42219T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6326T>A MANE Select ENSP00000495481.1:p.Phe2109Tyr
ENST00000205890.9:c.6326T>A ENSP00000205890.5:p.Phe2109Tyr
ENST00000615845.4:c.6326T>A ENSP00000481642.1:p.Phe2109Tyr
NM_016239.3:c.6326T>A NP_057323.3:p.Phe2109Tyr
XM_011523917.1:c.6266T>A XP_011522219.1:p.Phe2089Tyr
XM_011523918.1:c.6266T>A XP_011522220.1:p.Phe2089Tyr
XM_011523921.1:c.6320T>A XP_011522223.1:p.Phe2107Tyr
XR_934037.1:n.6925T>A
XR_934038.1:n.6925T>A
XM_011523918.2:c.6266T>A XP_011522220.1:p.Phe2089Tyr
XM_017024714.2:c.6266T>A XP_016880203.1:p.Phe2089Tyr
XM_017024715.2:c.6329T>A XP_016880204.1:p.Phe2110Tyr
XM_024450781.1:c.6213+1332T>A XP_024306549.1:n.6213+1332T>A
NM_016239.4:c.6326T>A MANE Select NP_057323.3:p.Phe2109Tyr
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