Canonical Allele Identifier: CA1897925678

Gene: MYO3A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26212360T= , CM000672.2:g.26212360T=	GRCh38
NC_000010.10:g.26501289T= , CM000672.1:g.26501289T=	GRCh37
NC_000010.9:g.26541295T=	NCBI36
NG_011635.1:g.283288T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642920.2:c.*397T= MANE Select	ENSP00000495965.1:n.*397T=
ENST00000645292.1:n.708T=
ENST00000265944.9:c.*397T=	ENSP00000265944.4:n.*397T=
NM_017433.4:c.*397T=	NP_059129.3:n.*397T=
XM_011519498.1:c.*397T=	XP_011517800.1:n.*397T=
XM_011519499.1:c.*397T=	XP_011517801.1:n.*397T=
XM_011519500.1:c.*397T=	XP_011517802.1:n.*397T=
XM_011519501.1:c.*397T=	XP_011517803.1:n.*397T=
XM_011519504.1:c.*299T=	XP_011517806.1:n.*299T=
XM_011519505.1:c.*397T=	XP_011517807.1:n.*397T=
XM_011519507.1:c.*397T=	XP_011517809.1:n.*397T=
XM_011519512.1:c.*397T=	XP_011517814.1:n.*397T=
XM_011519513.1:c.*397T=	XP_011517815.1:n.*397T=
XR_930493.1:n.5345T=
XM_011519498.2:c.*397T=	XP_011517800.1:n.*397T=
XM_011519500.2:c.*397T=	XP_011517802.1:n.*397T=
XM_011519513.2:c.*397T=	XP_011517815.1:n.*397T=
XR_001747111.1:n.4305T=
NM_017433.5:c.*397T= MANE Select	NP_059129.3:n.*397T=