Canonical Allele Identifier: CA1897925733

Gene: MYO3A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26212450G= , CM000672.2:g.26212450G=	GRCh38
NC_000010.10:g.26501379G= , CM000672.1:g.26501379G=	GRCh37
NC_000010.9:g.26541385G=	NCBI36
NG_011635.1:g.283378G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642920.2:c.*487G= MANE Select	ENSP00000495965.1:n.*487G=
ENST00000265944.9:c.*487G=	ENSP00000265944.4:n.*487G=
NM_017433.4:c.*487G=	NP_059129.3:n.*487G=
XM_011519498.1:c.*487G=	XP_011517800.1:n.*487G=
XM_011519499.1:c.*487G=	XP_011517801.1:n.*487G=
XM_011519500.1:c.*487G=	XP_011517802.1:n.*487G=
XM_011519501.1:c.*487G=	XP_011517803.1:n.*487G=
XM_011519504.1:c.*389G=	XP_011517806.1:n.*389G=
XM_011519505.1:c.*487G=	XP_011517807.1:n.*487G=
XM_011519507.1:c.*487G=	XP_011517809.1:n.*487G=
XM_011519512.1:c.*487G=	XP_011517814.1:n.*487G=
XM_011519513.1:c.*487G=	XP_011517815.1:n.*487G=
XR_930493.1:n.5435G=
XM_011519498.2:c.*487G=	XP_011517800.1:n.*487G=
XM_011519500.2:c.*487G=	XP_011517802.1:n.*487G=
XM_011519513.2:c.*487G=	XP_011517815.1:n.*487G=
XR_001747111.1:n.4395G=
NM_017433.5:c.*487G= MANE Select	NP_059129.3:n.*487G=