Canonical Allele Identifier: CA2250851764
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18149449A= , CM000679.2:g.18149449A= GRCh38
NC_000017.10:g.18052763A= , CM000679.1:g.18052763A= GRCh37
NC_000017.9:g.17993488A= NCBI36
NG_011634.1:g.45744A=
NG_011634.2:g.45744A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.7118-37A= MANE Select ENSP00000495481.1:n.7118-37A=
ENST00000205890.9:c.7118-37A= ENSP00000205890.5:n.7118-37A=
ENST00000578999.1:n.702A=
ENST00000615845.4:c.7118-37A= ENSP00000481642.1:n.7118-37A=
NM_016239.3:c.7118-37A= NP_057323.3:n.7118-37A=
XM_011523917.1:c.6793-37A= XP_011522219.1:n.6793-37A=
XM_011523921.1:c.7112-37A= XP_011522223.1:n.7112-37A=
XR_934037.1:n.7452-37A=
XR_934038.1:n.7404-37A=
XR_934293.1:n.435-1843T=
XR_934295.1:n.254-1843T=
XM_017024714.2:c.7058-37A= XP_016880203.1:n.7058-37A=
XM_017024715.2:c.7121-37A= XP_016880204.1:n.7121-37A=
XR_934293.2:n.378-1843T=
NM_016239.4:c.7118-37A= MANE Select NP_057323.3:n.7118-37A=