Canonical Allele Identifier: CA398607278
Gene: MYO15A HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.18049385T>A (hg19) chr17:g.18146071T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146071T>A , CM000679.2:g.18146071T>A GRCh38
NC_000017.10:g.18049385T>A , CM000679.1:g.18049385T>A GRCh37
NC_000017.9:g.17990110T>A NCBI36
NG_011634.1:g.42366T>A
NG_011634.2:g.42366T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6473T>A MANE Select ENSP00000495481.1:p.Phe2158Tyr
ENST00000205890.9:c.6473T>A ENSP00000205890.5:p.Phe2158Tyr
ENST00000578999.1:n.58T>A
ENST00000615845.4:c.6473T>A ENSP00000481642.1:p.Phe2158Tyr
NM_016239.3:c.6473T>A NP_057323.3:p.Phe2158Tyr
XM_011523917.1:c.6413T>A XP_011522219.1:p.Phe2138Tyr
XM_011523918.1:c.6342+71T>A XP_011522220.1:n.6342+71T>A
XM_011523921.1:c.6467T>A XP_011522223.1:p.Phe2156Tyr
XR_934037.1:n.7072T>A
XR_934038.1:n.7072T>A
XM_011523918.2:c.6342+71T>A XP_011522220.1:n.6342+71T>A
XM_017024714.2:c.6413T>A XP_016880203.1:p.Phe2138Tyr
XM_017024715.2:c.6476T>A XP_016880204.1:p.Phe2159Tyr
XM_024450781.1:c.6213+1479T>A XP_024306549.1:n.6213+1479T>A
NM_016239.4:c.6473T>A MANE Select NP_057323.3:p.Phe2158Tyr
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