Canonical Allele Identifier: CA385383356

Gene: MYO1A

Linked Data

• MyVariant Identifiers: chr12:g.57435230A>T (hg19) ; chr12:g.57041446A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57041446A>T , CM000674.2:g.57041446A>T	GRCh38
NC_000012.11:g.57435230A>T , CM000674.1:g.57435230A>T	GRCh37
NC_000012.10:g.55721497A>T	NCBI36
NG_012104.1:g.13664T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000300119.8:c.1150T>A MANE Select	ENSP00000300119.3:p.Phe384Ile
ENST00000300119.7:c.1150T>A	ENSP00000300119.3:p.Phe384Ile
ENST00000442789.6:c.1150T>A	ENSP00000393392.2:p.Phe384Ile
ENST00000554234.5:c.664T>A	ENSP00000451033.1:p.Phe222Ile
NM_001256041.1:c.1150T>A	NP_001242970.1:p.Phe384Ile
NM_005379.3:c.1150T>A	NP_005370.1:p.Phe384Ile
XM_011538373.1:c.1150T>A	XP_011536675.1:p.Phe384Ile
XM_011538373.2:c.1150T>A	XP_011536675.1:p.Phe384Ile
NM_005379.4:c.1150T>A MANE Select	NP_005370.1:p.Phe384Ile
NM_001256041.2:c.1150T>A	NP_001242970.1:p.Phe384Ile