Canonical Allele Identifier: CA2250851747
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18149421G= , CM000679.2:g.18149421G= GRCh38
NC_000017.10:g.18052735G= , CM000679.1:g.18052735G= GRCh37
NC_000017.9:g.17993460G= NCBI36
NG_011634.1:g.45716G=
NG_011634.2:g.45716G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.7117+45G= MANE Select ENSP00000495481.1:n.7117+45G=
ENST00000205890.9:c.7117+45G= ENSP00000205890.5:n.7117+45G=
ENST00000578999.1:n.674G=
ENST00000615845.4:c.7117+45G= ENSP00000481642.1:n.7117+45G=
NM_016239.3:c.7117+45G= NP_057323.3:n.7117+45G=
XM_011523917.1:c.6792+45G= XP_011522219.1:n.6792+45G=
XM_011523921.1:c.7111+45G= XP_011522223.1:n.7111+45G=
XR_934037.1:n.7451+45G=
XR_934038.1:n.7404-65G=
XR_934293.1:n.435-1815C=
XR_934295.1:n.254-1815C=
XM_017024714.2:c.7057+45G= XP_016880203.1:n.7057+45G=
XM_017024715.2:c.7120+45G= XP_016880204.1:n.7120+45G=
XR_934293.2:n.378-1815C=
NM_016239.4:c.7117+45G= MANE Select NP_057323.3:n.7117+45G=