Canonical Allele Identifier: CA8424576
Gene: MYO15A HGNC NCBI

Linked Data

ClinVar Variation Id: 1338933
ClinVar RCV Id: RCV001823387 RCV002542727
dbSNP Id: rs370756193
ExAC: 17:18049268 C / T
gnomAD v2: 17-18049268-C-T
gnomAD v3: 17-18145954-C-T
gnomAD v4: 17-18145954-C-T
MyVariant Identifiers: chr17:g.18049268C>T (hg19) chr17:g.18145954C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145954C>T , CM000679.2:g.18145954C>T GRCh38
NC_000017.10:g.18049268C>T , CM000679.1:g.18049268C>T GRCh37
NC_000017.9:g.17989993C>T NCBI36
NG_011634.1:g.42249C>T
NG_011634.2:g.42249C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6356C>T MANE Select ENSP00000495481.1:p.Ala2119Val
ENST00000205890.9:c.6356C>T ENSP00000205890.5:p.Ala2119Val
ENST00000615845.4:c.6356C>T ENSP00000481642.1:p.Ala2119Val
NM_016239.3:c.6356C>T NP_057323.3:p.Ala2119Val
XM_011523917.1:c.6296C>T XP_011522219.1:p.Ala2099Val
XM_011523918.1:c.6296C>T XP_011522220.1:p.Ala2099Val
XM_011523921.1:c.6350C>T XP_011522223.1:p.Ala2117Val
XR_934037.1:n.6955C>T
XR_934038.1:n.6955C>T
XM_011523918.2:c.6296C>T XP_011522220.1:p.Ala2099Val
XM_017024714.2:c.6296C>T XP_016880203.1:p.Ala2099Val
XM_017024715.2:c.6359C>T XP_016880204.1:p.Ala2120Val
XM_024450781.1:c.6213+1362C>T XP_024306549.1:n.6213+1362C>T
NM_016239.4:c.6356C>T MANE Select NP_057323.3:p.Ala2119Val
Search 100 bp 5'
Search 100 bp 3'