Canonical Allele Identifier: CA2250874564
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18159252G= , CM000679.2:g.18159252G= GRCh38
NC_000017.10:g.18062566G= , CM000679.1:g.18062566G= GRCh37
NC_000017.9:g.18003291G= NCBI36
NG_011634.1:g.55547G=
NG_011634.2:g.55547G=

Transcript Alleles

HGVS Amino-acid change
ENST00000642418.1:n.1495-23G=
ENST00000643693.1:n.959-23G=
ENST00000644795.1:c.949-23G= ENSP00000495720.1:n.949-23G=
ENST00000646782.1:n.1891-23G=
ENST00000647165.2:c.9157-23G= MANE Select ENSP00000495481.1:n.9157-23G=
ENST00000651214.1:n.1662-23G=
ENST00000205890.9:c.9157-23G= ENSP00000205890.5:n.9157-23G=
ENST00000418233.7:c.949-23G= ENSP00000408800.3:n.949-23G=
ENST00000433411.7:n.94-23G=
ENST00000445289.6:n.316+1352G=
ENST00000556535.5:c.19-23G= ENSP00000451782.1:n.19-23G=
ENST00000557190.5:n.59-23G=
ENST00000557655.5:c.19-23G= ENSP00000451925.1:n.19-23G=
ENST00000578472.5:c.19-23G= ENSP00000467989.1:n.19-23G=
ENST00000615845.4:c.9157-23G= ENSP00000481642.1:n.9157-23G=
NM_016239.3:c.9157-23G= NP_057323.3:n.9157-23G=
XM_011523921.1:c.9151-23G= XP_011522223.1:n.9151-23G=
XM_017024714.2:c.9097-23G= XP_016880203.1:n.9097-23G=
XM_017024715.2:c.9160-23G= XP_016880204.1:n.9160-23G=
NM_016239.4:c.9157-23G= MANE Select NP_057323.3:n.9157-23G=