Canonical Allele Identifier: CA361850016

Gene: GLRA1

Linked Data

• dbSNP Id: rs1581592489
• MyVariant Identifiers: chr5:g.151202398C>G (hg19) ; chr5:g.151822837C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151822837C>G , CM000667.2:g.151822837C>G	GRCh38
NC_000005.9:g.151202398C>G , CM000667.1:g.151202398C>G	GRCh37
NC_000005.8:g.151182591C>G	NCBI36
NG_011764.1:g.107000G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.1186G>C MANE Select	ENSP00000274576.5:p.Ala396Pro
ENST00000274576.8:c.1186G>C	ENSP00000274576.4:p.Ala396Pro
ENST00000455880.2:c.1210G>C	ENSP00000411593.2:p.Ala404Pro
ENST00000462581.6:c.*944G>C	ENSP00000430595.1:n.*944G>C
NM_000171.3:c.1186G>C	NP_000162.2:p.Ala396Pro
NM_001146040.1:c.1210G>C	NP_001139512.1:p.Ala404Pro
NM_001292000.1:c.937G>C	NP_001278929.1:p.Ala313Pro
NM_000171.4:c.1186G>C MANE Select	NP_000162.2:p.Ala396Pro
NM_001146040.2:c.1210G>C	NP_001139512.1:p.Ala404Pro
NM_001292000.2:c.937G>C	NP_001278929.1:p.Ala313Pro