Canonical Allele Identifier: CA398607275
Gene: MYO15A HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.18049384T>G (hg19) chr17:g.18146070T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146070T>G , CM000679.2:g.18146070T>G GRCh38
NC_000017.10:g.18049384T>G , CM000679.1:g.18049384T>G GRCh37
NC_000017.9:g.17990109T>G NCBI36
NG_011634.1:g.42365T>G
NG_011634.2:g.42365T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6472T>G MANE Select ENSP00000495481.1:p.Phe2158Val
ENST00000205890.9:c.6472T>G ENSP00000205890.5:p.Phe2158Val
ENST00000578999.1:n.57T>G
ENST00000615845.4:c.6472T>G ENSP00000481642.1:p.Phe2158Val
NM_016239.3:c.6472T>G NP_057323.3:p.Phe2158Val
XM_011523917.1:c.6412T>G XP_011522219.1:p.Phe2138Val
XM_011523918.1:c.6342+70T>G XP_011522220.1:n.6342+70T>G
XM_011523921.1:c.6466T>G XP_011522223.1:p.Phe2156Val
XR_934037.1:n.7071T>G
XR_934038.1:n.7071T>G
XM_011523918.2:c.6342+70T>G XP_011522220.1:n.6342+70T>G
XM_017024714.2:c.6412T>G XP_016880203.1:p.Phe2138Val
XM_017024715.2:c.6475T>G XP_016880204.1:p.Phe2159Val
XM_024450781.1:c.6213+1478T>G XP_024306549.1:n.6213+1478T>G
NM_016239.4:c.6472T>G MANE Select NP_057323.3:p.Phe2158Val
Search 100 bp 5'
Search 100 bp 3'