Canonical Allele Identifier: CA2038690630
Gene: MYO1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57041399G= , CM000674.2:g.57041399G= GRCh38
NC_000012.11:g.57435183G= , CM000674.1:g.57435183G= GRCh37
NC_000012.10:g.55721450G= NCBI36
NG_012104.1:g.13711C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300119.8:c.1164+33C= MANE Select ENSP00000300119.3:n.1164+33C=
ENST00000300119.7:c.1164+33C= ENSP00000300119.3:n.1164+33C=
ENST00000442789.6:c.1164+33C= ENSP00000393392.2:n.1164+33C=
ENST00000554234.5:c.678+33C= ENSP00000451033.1:n.678+33C=
NM_001256041.1:c.1164+33C= NP_001242970.1:n.1164+33C=
NM_005379.3:c.1164+33C= NP_005370.1:n.1164+33C=
XM_011538373.1:c.1164+33C= XP_011536675.1:n.1164+33C=
XM_011538373.2:c.1164+33C= XP_011536675.1:n.1164+33C=
NM_005379.4:c.1164+33C= MANE Select NP_005370.1:n.1164+33C=
NM_001256041.2:c.1164+33C= NP_001242970.1:n.1164+33C=