Canonical Allele Identifier: CA2250869135

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18157209C= , CM000679.2:g.18157209C=	GRCh38
NC_000017.10:g.18060523C= , CM000679.1:g.18060523C=	GRCh37
NC_000017.9:g.18001248C=	NCBI36
NG_011634.1:g.53504C=
NG_011634.2:g.53504C=

Transcript Alleles

HGVS	Amino-acid Change
NM_016239.4:c.8767C= MANE Select	NP_057323.3:p.Arg2923=
ENST00000647165.2:c.8767C= MANE Select	ENSP00000495481.1:p.Arg2923=
NM_016239.3:c.8767C=	NP_057323.3:p.Arg2923=
ENST00000205890.9:c.8767C=	ENSP00000205890.5:p.Arg2923=
ENST00000418233.7:c.559C=	ENSP00000408800.3:p.Arg187=
ENST00000445289.6:n.138-513C=
ENST00000536811.5:n.680C=
ENST00000615845.4:c.8767C=	ENSP00000481642.1:p.Arg2923=
ENST00000642418.1:n.614C=
ENST00000643693.1:n.587C=
ENST00000644795.1:c.559C=	ENSP00000495720.1:p.Arg187=
ENST00000646782.1:n.1010C=
ENST00000651214.1:n.913C=
XM_011523921.1:c.8761C=	XP_011522223.1:p.Arg2921=
XM_017024714.2:c.8707C=	XP_016880203.1:p.Arg2903=
XM_017024715.2:c.8770C=	XP_016880204.1:p.Arg2924=