Canonical Allele Identifier: CA398606482
Gene: MYO15A HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.18049231A>T (hg19) chr17:g.18145917A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145917A>T , CM000679.2:g.18145917A>T GRCh38
NC_000017.10:g.18049231A>T , CM000679.1:g.18049231A>T GRCh37
NC_000017.9:g.17989956A>T NCBI36
NG_011634.1:g.42212A>T
NG_011634.2:g.42212A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6319A>T MANE Select ENSP00000495481.1:p.Asn2107Tyr
ENST00000205890.9:c.6319A>T ENSP00000205890.5:p.Asn2107Tyr
ENST00000615845.4:c.6319A>T ENSP00000481642.1:p.Asn2107Tyr
NM_016239.3:c.6319A>T NP_057323.3:p.Asn2107Tyr
XM_011523917.1:c.6259A>T XP_011522219.1:p.Asn2087Tyr
XM_011523918.1:c.6259A>T XP_011522220.1:p.Asn2087Tyr
XM_011523921.1:c.6313A>T XP_011522223.1:p.Asn2105Tyr
XR_934037.1:n.6918A>T
XR_934038.1:n.6918A>T
XM_011523918.2:c.6259A>T XP_011522220.1:p.Asn2087Tyr
XM_017024714.2:c.6259A>T XP_016880203.1:p.Asn2087Tyr
XM_017024715.2:c.6322A>T XP_016880204.1:p.Asn2108Tyr
XM_024450781.1:c.6213+1325A>T XP_024306549.1:n.6213+1325A>T
NM_016239.4:c.6319A>T MANE Select NP_057323.3:p.Asn2107Tyr
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