Canonical Allele Identifier: CA1897908348

Gene: MYO3A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26125414C= , CM000672.2:g.26125414C=	GRCh38
NC_000010.10:g.26414343C= , CM000672.1:g.26414343C=	GRCh37
NC_000010.9:g.26454349C=	NCBI36
NG_011635.1:g.196342C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642197.1:n.2124C=
ENST00000642920.2:c.1920C= MANE Select	ENSP00000495965.1:p.Cys640=
ENST00000647478.1:c.1793C=	ENSP00000493932.1:p.Ala598=
ENST00000265944.9:c.1920C=	ENSP00000265944.4:p.Cys640=
ENST00000543632.5:c.1776+28732C=	ENSP00000445909.1:n.1776+28732C=
NM_017433.4:c.1920C=	NP_059129.3:p.Cys640=
XM_011519498.1:c.1920C=	XP_011517800.1:p.Cys640=
XM_011519499.1:c.1920C=	XP_011517801.1:p.Cys640=
XM_011519500.1:c.1920C=	XP_011517802.1:p.Cys640=
XM_011519501.1:c.1920C=	XP_011517803.1:p.Cys640=
XM_011519502.1:c.1920C=	XP_011517804.1:p.Cys640=
XM_011519503.1:c.1920C=	XP_011517805.1:p.Cys640=
XM_011519504.1:c.1920C=	XP_011517806.1:p.Cys640=
XM_011519505.1:c.1920C=	XP_011517807.1:p.Cys640=
XM_011519506.1:c.1920C=	XP_011517808.1:p.Cys640=
XM_011519507.1:c.1557C=	XP_011517809.1:p.Cys519=
XM_011519508.1:c.1920C=	XP_011517810.1:p.Cys640=
XM_011519509.1:c.1920C=	XP_011517811.1:p.Cys640=
XM_011519510.1:c.1920C=	XP_011517812.1:p.Cys640=
XM_011519511.1:c.1920C=	XP_011517813.1:p.Cys640=
XM_011519512.1:c.48C=	XP_011517814.1:p.Cys16=
XR_930492.1:n.2124C=
XR_930493.1:n.2124C=
XR_930494.1:n.2124C=
XM_011519498.2:c.1920C=	XP_011517800.1:p.Cys640=
XM_011519500.2:c.1920C=	XP_011517802.1:p.Cys640=
XM_011519506.2:c.1920C=	XP_011517808.1:p.Cys640=
XM_011519508.2:c.1920C=	XP_011517810.1:p.Cys640=
XM_011519510.2:c.1920C=	XP_011517812.1:p.Cys640=
XM_011519511.2:c.1920C=	XP_011517813.1:p.Cys640=
XR_001747111.1:n.2124C=
NM_017433.5:c.1920C= MANE Select	NP_059129.3:p.Cys640=