Canonical Allele Identifier: CA2038690515

Gene: MYO1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57041341T= , CM000674.2:g.57041341T=	GRCh38
NC_000012.11:g.57435125T= , CM000674.1:g.57435125T=	GRCh37
NC_000012.10:g.55721392T=	NCBI36
NG_012104.1:g.13769A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000300119.8:c.1165-53A= MANE Select	ENSP00000300119.3:n.1165-53A=
ENST00000300119.7:c.1165-53A=	ENSP00000300119.3:n.1165-53A=
ENST00000442789.6:c.1165-53A=	ENSP00000393392.2:n.1165-53A=
ENST00000554234.5:c.679-53A=	ENSP00000451033.1:n.679-53A=
NM_001256041.1:c.1165-53A=	NP_001242970.1:n.1165-53A=
NM_005379.3:c.1165-53A=	NP_005370.1:n.1165-53A=
XM_011538373.1:c.1165-53A=	XP_011536675.1:n.1165-53A=
XM_011538373.2:c.1165-53A=	XP_011536675.1:n.1165-53A=
NM_005379.4:c.1165-53A= MANE Select	NP_005370.1:n.1165-53A=
NM_001256041.2:c.1165-53A=	NP_001242970.1:n.1165-53A=