Canonical Allele Identifier: CA447224667
Gene: GLRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1752909824
MyVariant Identifiers: chr5:g.151231071G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151851510G>A , CM000667.2:g.151851510G>A GRCh38
NC_000005.9:g.151231071G>A , CM000667.1:g.151231071G>A GRCh37
NC_000005.8:g.151211264G>A NCBI36
NG_011764.1:g.78327C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274576.9:c.792C>T MANE Select ENSP00000274576.5:p.Ile264=
ENST00000274576.8:c.792C>T ENSP00000274576.4:p.Ile264=
ENST00000455880.2:c.792C>T ENSP00000411593.2:p.Ile264=
ENST00000462581.6:c.*550C>T ENSP00000430595.1:n.*550C>T
ENST00000471351.2:n.1075C>T
NM_000171.3:c.792C>T NP_000162.2:p.Ile264=
NM_001146040.1:c.792C>T NP_001139512.1:p.Ile264=
NM_001292000.1:c.543C>T NP_001278929.1:p.Ile181=
XM_005268412.2:c.792C>T XP_005268469.1:p.Ile264=
NM_000171.4:c.792C>T MANE Select NP_000162.2:p.Ile264=
NM_001146040.2:c.792C>T NP_001139512.1:p.Ile264=
NM_001292000.2:c.543C>T NP_001278929.1:p.Ile181=