Canonical Allele Identifier: CA2250851766
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18149458C= , CM000679.2:g.18149458C= GRCh38
NC_000017.10:g.18052772C= , CM000679.1:g.18052772C= GRCh37
NC_000017.9:g.17993497C= NCBI36
NG_011634.1:g.45753C=
NG_011634.2:g.45753C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.7118-28C= MANE Select ENSP00000495481.1:n.7118-28C=
ENST00000205890.9:c.7118-28C= ENSP00000205890.5:n.7118-28C=
ENST00000578999.1:n.711C=
ENST00000615845.4:c.7118-28C= ENSP00000481642.1:n.7118-28C=
NM_016239.3:c.7118-28C= NP_057323.3:n.7118-28C=
XM_011523917.1:c.6793-28C= XP_011522219.1:n.6793-28C=
XM_011523921.1:c.7112-28C= XP_011522223.1:n.7112-28C=
XR_934037.1:n.7452-28C=
XR_934038.1:n.7404-28C=
XR_934293.1:n.435-1852G=
XR_934295.1:n.254-1852G=
XM_017024714.2:c.7058-28C= XP_016880203.1:n.7058-28C=
XM_017024715.2:c.7121-28C= XP_016880204.1:n.7121-28C=
XR_934293.2:n.378-1852G=
NM_016239.4:c.7118-28C= MANE Select NP_057323.3:n.7118-28C=