Canonical Allele Identifier: CA2840524865
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18149434dup , CM000679.2:g.18149434dup GRCh38
NC_000017.10:g.18052748dup , CM000679.1:g.18052748dup GRCh37
NC_000017.9:g.17993473dup NCBI36
NG_011634.1:g.45729dup
NG_011634.2:g.45729dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.7118-52dup MANE Select ENSP00000495481.1:n.7118-52dup
ENST00000205890.9:c.7118-52dup ENSP00000205890.5:n.7118-52dup
ENST00000578999.1:n.687dup
ENST00000615845.4:c.7118-52dup ENSP00000481642.1:n.7118-52dup
NM_016239.3:c.7118-52dup NP_057323.3:n.7118-52dup
XM_011523917.1:c.6793-52dup XP_011522219.1:n.6793-52dup
XM_011523921.1:c.7112-52dup XP_011522223.1:n.7112-52dup
XR_934037.1:n.7452-52dup
XR_934038.1:n.7404-52dup
XR_934293.1:n.435-1825dup
XR_934295.1:n.254-1825dup
XM_017024714.2:c.7058-52dup XP_016880203.1:n.7058-52dup
XM_017024715.2:c.7121-52dup XP_016880204.1:n.7121-52dup
XR_934293.2:n.378-1825dup
NM_016239.4:c.7118-52dup MANE Select NP_057323.3:n.7118-52dup