Canonical Allele Identifier: CA2250882574

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18163251G= , CM000679.2:g.18163251G=	GRCh38
NC_000017.10:g.18066565G= , CM000679.1:g.18066565G=	GRCh37
NC_000017.9:g.18007290G=	NCBI36
NG_011634.1:g.59546G=
NG_011634.2:g.59546G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1884G=
ENST00000643693.1:n.1422G=
ENST00000644795.1:c.1412G=	ENSP00000495720.1:p.Arg471=
ENST00000646782.1:n.2354G=
ENST00000647165.2:c.9620G= MANE Select	ENSP00000495481.1:p.Arg3207=
ENST00000651214.1:n.2051G=
ENST00000205890.9:c.9620G=	ENSP00000205890.5:p.Arg3207=
ENST00000418233.7:c.1412G=	ENSP00000408800.3:p.Arg471=
ENST00000433411.7:n.1070G=
ENST00000445289.6:n.550G=
ENST00000473013.1:n.804G=
ENST00000557190.5:n.448G=
ENST00000557655.5:c.*300G=	ENSP00000451925.1:n.*300G=
ENST00000578575.1:c.183G=
ENST00000579848.6:c.335G=	ENSP00000465910.1:p.Arg112=
ENST00000615845.4:c.9620G=	ENSP00000481642.1:p.Arg3207=
NM_016239.3:c.9620G=	NP_057323.3:p.Arg3207=
XM_011523921.1:c.9614G=	XP_011522223.1:p.Arg3205=
XM_017024714.2:c.9560G=	XP_016880203.1:p.Arg3187=
XM_017024715.2:c.9623G=	XP_016880204.1:p.Arg3208=
NM_016239.4:c.9620G= MANE Select	NP_057323.3:p.Arg3207=