Canonical Allele Identifier: CA726643766
Gene: MYO15A HGNC NCBI

Linked Data

dbSNP Id: rs1470674624
gnomAD v3: 17-18145688-C-A
gnomAD v4: 17-18145688-C-A
MyVariant Identifiers: chr17:g.18049002C>A (hg19) chr17:g.18145688C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145688C>A , CM000679.2:g.18145688C>A GRCh38
NC_000017.10:g.18049002C>A , CM000679.1:g.18049002C>A GRCh37
NC_000017.9:g.17989727C>A NCBI36
NG_011634.1:g.41983C>A
NG_011634.2:g.41983C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6274-184C>A MANE Select ENSP00000495481.1:n.6274-184C>A
ENST00000205890.9:c.6274-184C>A ENSP00000205890.5:n.6274-184C>A
ENST00000615845.4:c.6274-184C>A ENSP00000481642.1:n.6274-184C>A
NM_016239.3:c.6274-184C>A NP_057323.3:n.6274-184C>A
XM_011523917.1:c.6214-184C>A XP_011522219.1:n.6214-184C>A
XM_011523918.1:c.6214-184C>A XP_011522220.1:n.6214-184C>A
XM_011523921.1:c.6268-184C>A XP_011522223.1:n.6268-184C>A
XR_934037.1:n.6873-184C>A
XR_934038.1:n.6873-184C>A
XM_011523918.2:c.6214-184C>A XP_011522220.1:n.6214-184C>A
XM_017024714.2:c.6214-184C>A XP_016880203.1:n.6214-184C>A
XM_017024715.2:c.6277-184C>A XP_016880204.1:n.6277-184C>A
XM_024450781.1:c.6213+1096C>A XP_024306549.1:n.6213+1096C>A
NM_016239.4:c.6274-184C>A MANE Select NP_057323.3:n.6274-184C>A
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