Canonical Allele Identifier: CA2836791838
Gene: MYO15A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146162A>T , CM000679.2:g.18146162A>T GRCh38
NC_000017.10:g.18049476A>T , CM000679.1:g.18049476A>T GRCh37
NC_000017.9:g.17990201A>T NCBI36
NG_011634.1:g.42457A>T
NG_011634.2:g.42457A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6509+55A>T MANE Select ENSP00000495481.1:n.6509+55A>T
ENST00000205890.9:c.6509+55A>T ENSP00000205890.5:n.6509+55A>T
ENST00000578999.1:n.94+55A>T
ENST00000615845.4:c.6509+55A>T ENSP00000481642.1:n.6509+55A>T
NM_016239.3:c.6509+55A>T NP_057323.3:n.6509+55A>T
XM_011523917.1:c.6449+55A>T XP_011522219.1:n.6449+55A>T
XM_011523918.1:c.6342+162A>T XP_011522220.1:n.6342+162A>T
XM_011523921.1:c.6503+55A>T XP_011522223.1:n.6503+55A>T
XR_934037.1:n.7108+55A>T
XR_934038.1:n.7108+55A>T
XM_011523918.2:c.6342+162A>T XP_011522220.1:n.6342+162A>T
XM_017024714.2:c.6449+55A>T XP_016880203.1:n.6449+55A>T
XM_017024715.2:c.6512+55A>T XP_016880204.1:n.6512+55A>T
XM_024450781.1:c.6213+1570A>T XP_024306549.1:n.6213+1570A>T
NM_016239.4:c.6509+55A>T MANE Select NP_057323.3:n.6509+55A>T
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