Canonical Allele Identifier: CA2038690559
Gene: MYO1A HGNC NCBI

Linked Data

dbSNP Id: rs2030850642

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57041368C>A , CM000674.2:g.57041368C>A GRCh38
NC_000012.11:g.57435152C>A , CM000674.1:g.57435152C>A GRCh37
NC_000012.10:g.55721419C>A NCBI36
NG_012104.1:g.13742G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000300119.8:c.1164+64G>T MANE Select ENSP00000300119.3:n.1164+64G>T
ENST00000300119.7:c.1164+64G>T ENSP00000300119.3:n.1164+64G>T
ENST00000442789.6:c.1164+64G>T ENSP00000393392.2:n.1164+64G>T
ENST00000554234.5:c.678+64G>T ENSP00000451033.1:n.678+64G>T
NM_001256041.1:c.1164+64G>T NP_001242970.1:n.1164+64G>T
NM_005379.3:c.1164+64G>T NP_005370.1:n.1164+64G>T
XM_011538373.1:c.1164+64G>T XP_011536675.1:n.1164+64G>T
XM_011538373.2:c.1164+64G>T XP_011536675.1:n.1164+64G>T
NM_005379.4:c.1164+64G>T MANE Select NP_005370.1:n.1164+64G>T
NM_001256041.2:c.1164+64G>T NP_001242970.1:n.1164+64G>T