Canonical Allele Identifier: CA1897925685

Gene: MYO3A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26212365T= , CM000672.2:g.26212365T=	GRCh38
NC_000010.10:g.26501294T= , CM000672.1:g.26501294T=	GRCh37
NC_000010.9:g.26541300T=	NCBI36
NG_011635.1:g.283293T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642920.2:c.*402T= MANE Select	ENSP00000495965.1:n.*402T=
ENST00000645292.1:n.713T=
ENST00000265944.9:c.*402T=	ENSP00000265944.4:n.*402T=
NM_017433.4:c.*402T=	NP_059129.3:n.*402T=
XM_011519498.1:c.*402T=	XP_011517800.1:n.*402T=
XM_011519499.1:c.*402T=	XP_011517801.1:n.*402T=
XM_011519500.1:c.*402T=	XP_011517802.1:n.*402T=
XM_011519501.1:c.*402T=	XP_011517803.1:n.*402T=
XM_011519504.1:c.*304T=	XP_011517806.1:n.*304T=
XM_011519505.1:c.*402T=	XP_011517807.1:n.*402T=
XM_011519507.1:c.*402T=	XP_011517809.1:n.*402T=
XM_011519512.1:c.*402T=	XP_011517814.1:n.*402T=
XM_011519513.1:c.*402T=	XP_011517815.1:n.*402T=
XR_930493.1:n.5350T=
XM_011519498.2:c.*402T=	XP_011517800.1:n.*402T=
XM_011519500.2:c.*402T=	XP_011517802.1:n.*402T=
XM_011519513.2:c.*402T=	XP_011517815.1:n.*402T=
XR_001747111.1:n.4310T=
NM_017433.5:c.*402T= MANE Select	NP_059129.3:n.*402T=