Canonical Allele Identifier: CA2250851465
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18148784G= , CM000679.2:g.18148784G= GRCh38
NC_000017.10:g.18052098G= , CM000679.1:g.18052098G= GRCh37
NC_000017.9:g.17992823G= NCBI36
NG_011634.1:g.45079G=
NG_011634.2:g.45079G=

Transcript Alleles

HGVS Amino-acid Change
NM_016239.4:c.6788G= MANE Select NP_057323.3:p.Gly2263=
ENST00000647165.2:c.6788G= MANE Select ENSP00000495481.1:p.Gly2263=
NM_016239.3:c.6788G= NP_057323.3:p.Gly2263=
ENST00000205890.9:c.6788G= ENSP00000205890.5:p.Gly2263=
ENST00000578999.1:n.300G=
ENST00000615845.4:c.6788G= ENSP00000481642.1:p.Gly2263=
XM_011523917.1:c.6632-432G= XP_011522219.1:n.6632-432G=
XM_011523921.1:c.6782G= XP_011522223.1:p.Gly2261=
XM_017024714.2:c.6728G= XP_016880203.1:p.Gly2243=
XM_017024715.2:c.6791G= XP_016880204.1:p.Gly2264=
XR_934037.1:n.7291-432G=
XR_934038.1:n.7291-432G=
XR_934293.1:n.435-1178C=
XR_934293.2:n.378-1178C=
XR_934295.1:n.254-1178C=