Canonical Allele Identifier: CA1897913679

Gene: MYO3A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26170557C= , CM000672.2:g.26170557C=	GRCh38
NC_000010.10:g.26459486C= , CM000672.1:g.26459486C=	GRCh37
NC_000010.9:g.26499492C=	NCBI36
NG_011635.1:g.241485C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000642920.2:c.3398+18C= MANE Select	ENSP00000495965.1:n.3398+18C=
ENST00000647478.1:c.*1393+18C=	ENSP00000493932.1:n.*1393+18C=
ENST00000265944.9:c.3398+18C=	ENSP00000265944.4:n.3398+18C=
ENST00000543632.5:c.1777-41286C=	ENSP00000445909.1:n.1777-41286C=
NM_017433.4:c.3398+18C=	NP_059129.3:n.3398+18C=
XM_011519498.1:c.3398+18C=	XP_011517800.1:n.3398+18C=
XM_011519499.1:c.3398+18C=	XP_011517801.1:n.3398+18C=
XM_011519500.1:c.3398+18C=	XP_011517802.1:n.3398+18C=
XM_011519501.1:c.3398+18C=	XP_011517803.1:n.3398+18C=
XM_011519502.1:c.3398+18C=	XP_011517804.1:n.3398+18C=
XM_011519503.1:c.3398+18C=	XP_011517805.1:n.3398+18C=
XM_011519504.1:c.3398+18C=	XP_011517806.1:n.3398+18C=
XM_011519505.1:c.3398+18C=	XP_011517807.1:n.3398+18C=
XM_011519506.1:c.3398+18C=	XP_011517808.1:n.3398+18C=
XM_011519507.1:c.3035+18C=	XP_011517809.1:n.3035+18C=
XM_011519508.1:c.3398+18C=	XP_011517810.1:n.3398+18C=
XM_011519509.1:c.3398+18C=	XP_011517811.1:n.3398+18C=
XM_011519510.1:c.3398+18C=	XP_011517812.1:n.3398+18C=
XM_011519512.1:c.1526+18C=	XP_011517814.1:n.1526+18C=
XM_011519513.1:c.1067+18C=	XP_011517815.1:n.1067+18C=
XR_930492.1:n.3602+18C=
XR_930493.1:n.3602+18C=
XR_930494.1:n.3602+18C=
XM_011519498.2:c.3398+18C=	XP_011517800.1:n.3398+18C=
XM_011519500.2:c.3398+18C=	XP_011517802.1:n.3398+18C=
XM_011519506.2:c.3398+18C=	XP_011517808.1:n.3398+18C=
XM_011519508.2:c.3398+18C=	XP_011517810.1:n.3398+18C=
XM_011519510.2:c.3398+18C=	XP_011517812.1:n.3398+18C=
XM_011519513.2:c.1067+18C=	XP_011517815.1:n.1067+18C=
XR_001747111.1:n.3602+18C=
NM_017433.5:c.3398+18C= MANE Select	NP_059129.3:n.3398+18C=