Canonical Allele Identifier: CA237704025

Gene: MYO1A

Linked Data

• dbSNP Id: rs984342424
• MyVariant Identifiers: chr12:g.57435236A>G (hg19) ; chr12:g.57041452A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57041452A>G , CM000674.2:g.57041452A>G	GRCh38
NC_000012.11:g.57435236A>G , CM000674.1:g.57435236A>G	GRCh37
NC_000012.10:g.55721503A>G	NCBI36
NG_012104.1:g.13658T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000300119.8:c.1144T>C MANE Select	ENSP00000300119.3:p.Tyr382His
ENST00000300119.7:c.1144T>C	ENSP00000300119.3:p.Tyr382His
ENST00000442789.6:c.1144T>C	ENSP00000393392.2:p.Tyr382His
ENST00000554234.5:c.658T>C	ENSP00000451033.1:p.Tyr220His
NM_001256041.1:c.1144T>C	NP_001242970.1:p.Tyr382His
NM_005379.3:c.1144T>C	NP_005370.1:p.Tyr382His
XM_011538373.1:c.1144T>C	XP_011536675.1:p.Tyr382His
XM_011538373.2:c.1144T>C	XP_011536675.1:p.Tyr382His
NM_005379.4:c.1144T>C MANE Select	NP_005370.1:p.Tyr382His
NM_001256041.2:c.1144T>C	NP_001242970.1:p.Tyr382His