Canonical Allele Identifier: CA398606455
Gene: MYO15A HGNC NCBI

Linked Data

gnomAD v4: 17-18145909-C-T
MyVariant Identifiers: chr17:g.18049223C>T (hg19) chr17:g.18145909C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145909C>T , CM000679.2:g.18145909C>T GRCh38
NC_000017.10:g.18049223C>T , CM000679.1:g.18049223C>T GRCh37
NC_000017.9:g.17989948C>T NCBI36
NG_011634.1:g.42204C>T
NG_011634.2:g.42204C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6311C>T MANE Select ENSP00000495481.1:p.Ala2104Val
ENST00000205890.9:c.6311C>T ENSP00000205890.5:p.Ala2104Val
ENST00000615845.4:c.6311C>T ENSP00000481642.1:p.Ala2104Val
NM_016239.3:c.6311C>T NP_057323.3:p.Ala2104Val
XM_011523917.1:c.6251C>T XP_011522219.1:p.Ala2084Val
XM_011523918.1:c.6251C>T XP_011522220.1:p.Ala2084Val
XM_011523921.1:c.6305C>T XP_011522223.1:p.Ala2102Val
XR_934037.1:n.6910C>T
XR_934038.1:n.6910C>T
XM_011523918.2:c.6251C>T XP_011522220.1:p.Ala2084Val
XM_017024714.2:c.6251C>T XP_016880203.1:p.Ala2084Val
XM_017024715.2:c.6314C>T XP_016880204.1:p.Ala2105Val
XM_024450781.1:c.6213+1317C>T XP_024306549.1:n.6213+1317C>T
NM_016239.4:c.6311C>T MANE Select NP_057323.3:p.Ala2104Val
Search 100 bp 5'
Search 100 bp 3'