Canonical Allele Identifier: CA2250874441
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18159194T= , CM000679.2:g.18159194T= GRCh38
NC_000017.10:g.18062508T= , CM000679.1:g.18062508T= GRCh37
NC_000017.9:g.18003233T= NCBI36
NG_011634.1:g.55489T=
NG_011634.2:g.55489T=

Transcript Alleles

HGVS Amino-acid change
ENST00000642418.1:n.1495-81T=
ENST00000643693.1:n.959-81T=
ENST00000644795.1:c.949-81T= ENSP00000495720.1:n.949-81T=
ENST00000646782.1:n.1891-81T=
ENST00000647165.2:c.9157-81T= MANE Select ENSP00000495481.1:n.9157-81T=
ENST00000651214.1:n.1662-81T=
ENST00000205890.9:c.9157-81T= ENSP00000205890.5:n.9157-81T=
ENST00000418233.7:c.949-81T= ENSP00000408800.3:n.949-81T=
ENST00000433411.7:n.94-81T=
ENST00000445289.6:n.316+1294T=
ENST00000556535.5:c.19-81T= ENSP00000451782.1:n.19-81T=
ENST00000557190.5:n.59-81T=
ENST00000557655.5:c.19-81T= ENSP00000451925.1:n.19-81T=
ENST00000578472.5:c.19-81T= ENSP00000467989.1:n.19-81T=
ENST00000615845.4:c.9157-81T= ENSP00000481642.1:n.9157-81T=
NM_016239.3:c.9157-81T= NP_057323.3:n.9157-81T=
XM_011523921.1:c.9151-81T= XP_011522223.1:n.9151-81T=
XM_017024714.2:c.9097-81T= XP_016880203.1:n.9097-81T=
XM_017024715.2:c.9160-81T= XP_016880204.1:n.9160-81T=
NM_016239.4:c.9157-81T= MANE Select NP_057323.3:n.9157-81T=