Canonical Allele Identifier: CA1897925676

Gene: MYO3A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26212358T= , CM000672.2:g.26212358T=	GRCh38
NC_000010.10:g.26501287T= , CM000672.1:g.26501287T=	GRCh37
NC_000010.9:g.26541293T=	NCBI36
NG_011635.1:g.283286T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642920.2:c.*395T= MANE Select	ENSP00000495965.1:n.*395T=
ENST00000645292.1:n.706T=
ENST00000265944.9:c.*395T=	ENSP00000265944.4:n.*395T=
NM_017433.4:c.*395T=	NP_059129.3:n.*395T=
XM_011519498.1:c.*395T=	XP_011517800.1:n.*395T=
XM_011519499.1:c.*395T=	XP_011517801.1:n.*395T=
XM_011519500.1:c.*395T=	XP_011517802.1:n.*395T=
XM_011519501.1:c.*395T=	XP_011517803.1:n.*395T=
XM_011519504.1:c.*297T=	XP_011517806.1:n.*297T=
XM_011519505.1:c.*395T=	XP_011517807.1:n.*395T=
XM_011519507.1:c.*395T=	XP_011517809.1:n.*395T=
XM_011519512.1:c.*395T=	XP_011517814.1:n.*395T=
XM_011519513.1:c.*395T=	XP_011517815.1:n.*395T=
XR_930493.1:n.5343T=
XM_011519498.2:c.*395T=	XP_011517800.1:n.*395T=
XM_011519500.2:c.*395T=	XP_011517802.1:n.*395T=
XM_011519513.2:c.*395T=	XP_011517815.1:n.*395T=
XR_001747111.1:n.4303T=
NM_017433.5:c.*395T= MANE Select	NP_059129.3:n.*395T=