Canonical Allele Identifier: CA2250849410

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18143717G= , CM000679.2:g.18143717G=	GRCh38
NC_000017.10:g.18047031G= , CM000679.1:g.18047031G=	GRCh37
NC_000017.9:g.17987756G=	NCBI36
NG_011634.1:g.40012G=
NG_011634.2:g.40012G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647165.2:c.5967G= MANE Select	ENSP00000495481.1:p.Glu1989=
ENST00000205890.9:c.5967G=	ENSP00000205890.5:p.Glu1989=
ENST00000615845.4:c.5967G=	ENSP00000481642.1:p.Glu1989=
NM_016239.3:c.5967G=	NP_057323.3:p.Glu1989=
XM_011523917.1:c.5907G=	XP_011522219.1:p.Glu1969=
XM_011523918.1:c.5907G=	XP_011522220.1:p.Glu1969=
XM_011523919.1:c.5907G=	XP_011522221.1:p.Glu1969=
XM_011523920.1:c.*169G=	XP_011522222.1:n.*169G=
XM_011523921.1:c.5961G=	XP_011522223.1:p.Glu1987=
XR_934037.1:n.6566G=
XR_934038.1:n.6566G=
XR_934039.1:n.6859G=
XM_011523918.2:c.5907G=	XP_011522220.1:p.Glu1969=
XM_017024714.2:c.5907G=	XP_016880203.1:p.Glu1969=
XM_017024715.2:c.5970G=	XP_016880204.1:p.Glu1990=
XM_024450780.1:c.5907G=	XP_024306548.1:p.Glu1969=
XM_024450781.1:c.5907G=	XP_024306549.1:p.Glu1969=
XM_024450782.1:c.*169G=	XP_024306550.1:n.*169G=
XR_934039.2:n.6898G=
NM_016239.4:c.5967G= MANE Select	NP_057323.3:p.Glu1989=