Canonical Allele Identifier: CA8424592
Gene: MYO15A HGNC NCBI

Linked Data

ClinVar Variation Id: 1687646
ClinVar RCV Id: RCV002251620
dbSNP Id: rs779026723
ExAC: 17:18049375 C / T
gnomAD v2: 17-18049375-C-T
gnomAD v3: 17-18146061-C-T
gnomAD v4: 17-18146061-C-T
MyVariant Identifiers: chr17:g.18049375C>T (hg19) chr17:g.18146061C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146061C>T , CM000679.2:g.18146061C>T GRCh38
NC_000017.10:g.18049375C>T , CM000679.1:g.18049375C>T GRCh37
NC_000017.9:g.17990100C>T NCBI36
NG_011634.1:g.42356C>T
NG_011634.2:g.42356C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6463C>T MANE Select ENSP00000495481.1:p.Leu2155Phe
ENST00000205890.9:c.6463C>T ENSP00000205890.5:p.Leu2155Phe
ENST00000578999.1:n.48C>T
ENST00000615845.4:c.6463C>T ENSP00000481642.1:p.Leu2155Phe
NM_016239.3:c.6463C>T NP_057323.3:p.Leu2155Phe
XM_011523917.1:c.6403C>T XP_011522219.1:p.Leu2135Phe
XM_011523918.1:c.6342+61C>T XP_011522220.1:n.6342+61C>T
XM_011523921.1:c.6457C>T XP_011522223.1:p.Leu2153Phe
XR_934037.1:n.7062C>T
XR_934038.1:n.7062C>T
XM_011523918.2:c.6342+61C>T XP_011522220.1:n.6342+61C>T
XM_017024714.2:c.6403C>T XP_016880203.1:p.Leu2135Phe
XM_017024715.2:c.6466C>T XP_016880204.1:p.Leu2156Phe
XM_024450781.1:c.6213+1469C>T XP_024306549.1:n.6213+1469C>T
NM_016239.4:c.6463C>T MANE Select NP_057323.3:p.Leu2155Phe
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