Canonical Allele Identifier: CA2576190423
Gene: MYO15A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146160G>A , CM000679.2:g.18146160G>A GRCh38
NC_000017.10:g.18049474G>A , CM000679.1:g.18049474G>A GRCh37
NC_000017.9:g.17990199G>A NCBI36
NG_011634.1:g.42455G>A
NG_011634.2:g.42455G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6509+53G>A MANE Select ENSP00000495481.1:n.6509+53G>A
ENST00000205890.9:c.6509+53G>A ENSP00000205890.5:n.6509+53G>A
ENST00000578999.1:n.94+53G>A
ENST00000615845.4:c.6509+53G>A ENSP00000481642.1:n.6509+53G>A
NM_016239.3:c.6509+53G>A NP_057323.3:n.6509+53G>A
XM_011523917.1:c.6449+53G>A XP_011522219.1:n.6449+53G>A
XM_011523918.1:c.6342+160G>A XP_011522220.1:n.6342+160G>A
XM_011523921.1:c.6503+53G>A XP_011522223.1:n.6503+53G>A
XR_934037.1:n.7108+53G>A
XR_934038.1:n.7108+53G>A
XM_011523918.2:c.6342+160G>A XP_011522220.1:n.6342+160G>A
XM_017024714.2:c.6449+53G>A XP_016880203.1:n.6449+53G>A
XM_017024715.2:c.6512+53G>A XP_016880204.1:n.6512+53G>A
XM_024450781.1:c.6213+1568G>A XP_024306549.1:n.6213+1568G>A
NM_016239.4:c.6509+53G>A MANE Select NP_057323.3:n.6509+53G>A
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