Canonical Allele Identifier: CA948050616
Gene: MYO1A HGNC NCBI

Linked Data

dbSNP Id: rs2030850068

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57041346C>A , CM000674.2:g.57041346C>A GRCh38
NC_000012.11:g.57435130C>A , CM000674.1:g.57435130C>A GRCh37
NC_000012.10:g.55721397C>A NCBI36
NG_012104.1:g.13764G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000300119.8:c.1165-58G>T MANE Select ENSP00000300119.3:n.1165-58G>T
ENST00000300119.7:c.1165-58G>T ENSP00000300119.3:n.1165-58G>T
ENST00000442789.6:c.1165-58G>T ENSP00000393392.2:n.1165-58G>T
ENST00000554234.5:c.679-58G>T ENSP00000451033.1:n.679-58G>T
NM_001256041.1:c.1165-58G>T NP_001242970.1:n.1165-58G>T
NM_005379.3:c.1165-58G>T NP_005370.1:n.1165-58G>T
XM_011538373.1:c.1165-58G>T XP_011536675.1:n.1165-58G>T
XM_011538373.2:c.1165-58G>T XP_011536675.1:n.1165-58G>T
NM_005379.4:c.1165-58G>T MANE Select NP_005370.1:n.1165-58G>T
NM_001256041.2:c.1165-58G>T NP_001242970.1:n.1165-58G>T