Canonical Allele Identifier: CA237703862

Gene: MYO1A

Linked Data

• dbSNP Id: rs190177249
• gnomAD v3: 12-57041341-T-C
• gnomAD v4: 12-57041341-T-C
• MyVariant Identifiers: chr12:g.57435125T>C (hg19) ; chr12:g.57041341T>C (hg38)

Genomic Alleles

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

Transcript Alleles

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