Canonical Allele Identifier: CA2038684600
Community Standard Title: NM_005379.4(MYO1A):c.1985G= (p.Gly662=)
Gene: MYO1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57037618C= , CM000674.2:g.57037618C= GRCh38
NC_000012.11:g.57431402C= , CM000674.1:g.57431402C= GRCh37
NC_000012.10:g.55717669C= NCBI36
NG_012104.1:g.17492G=

Transcript Alleles

HGVS Amino-acid Change
NM_005379.4:c.1985G= MANE Select NP_005370.1:p.Gly662=
ENST00000300119.8:c.1985G= MANE Select ENSP00000300119.3:p.Gly662=
NM_001256041.1:c.1985G= NP_001242970.1:p.Gly662=
NM_001256041.2:c.1985G= NP_001242970.1:p.Gly662=
NM_005379.3:c.1985G= NP_005370.1:p.Gly662=
ENST00000300119.7:c.1985G= ENSP00000300119.3:p.Gly662=
ENST00000442789.6:c.1985G= ENSP00000393392.2:p.Gly662=
ENST00000554234.5:c.1499G= ENSP00000451033.1:p.Gly500=
XM_011538373.1:c.1985G= XP_011536675.1:p.Gly662=
XM_011538373.2:c.1985G= XP_011536675.1:p.Gly662=