Canonical Allele Identifier: CA2808665080
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18149431G>T , CM000679.2:g.18149431G>T GRCh38
NC_000017.10:g.18052745G>T , CM000679.1:g.18052745G>T GRCh37
NC_000017.9:g.17993470G>T NCBI36
NG_011634.1:g.45726G>T
NG_011634.2:g.45726G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.7118-55G>T MANE Select ENSP00000495481.1:n.7118-55G>T
ENST00000205890.9:c.7118-55G>T ENSP00000205890.5:n.7118-55G>T
ENST00000578999.1:n.684G>T
ENST00000615845.4:c.7118-55G>T ENSP00000481642.1:n.7118-55G>T
NM_016239.3:c.7118-55G>T NP_057323.3:n.7118-55G>T
XM_011523917.1:c.6793-55G>T XP_011522219.1:n.6793-55G>T
XM_011523921.1:c.7112-55G>T XP_011522223.1:n.7112-55G>T
XR_934037.1:n.7452-55G>T
XR_934038.1:n.7404-55G>T
XR_934293.1:n.435-1825C>A
XR_934295.1:n.254-1825C>A
XM_017024714.2:c.7058-55G>T XP_016880203.1:n.7058-55G>T
XM_017024715.2:c.7121-55G>T XP_016880204.1:n.7121-55G>T
XR_934293.2:n.378-1825C>A
NM_016239.4:c.7118-55G>T MANE Select NP_057323.3:n.7118-55G>T