Canonical Allele Identifier: CA130006426

Gene: GLRA1

Linked Data

• dbSNP Id: rs931705728
• MyVariant Identifiers: chr5:g.151202496T>G (hg19) ; chr5:g.151822935T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151822935T>G , CM000667.2:g.151822935T>G	GRCh38
NC_000005.9:g.151202496T>G , CM000667.1:g.151202496T>G	GRCh37
NC_000005.8:g.151182689T>G	NCBI36
NG_011764.1:g.106902A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.1088A>C MANE Select	ENSP00000274576.5:p.Asn363Thr
ENST00000274576.8:c.1088A>C	ENSP00000274576.4:p.Asn363Thr
ENST00000455880.2:c.1112A>C	ENSP00000411593.2:p.Asn371Thr
ENST00000462581.6:c.*846A>C	ENSP00000430595.1:n.*846A>C
NM_000171.3:c.1088A>C	NP_000162.2:p.Asn363Thr
NM_001146040.1:c.1112A>C	NP_001139512.1:p.Asn371Thr
NM_001292000.1:c.839A>C	NP_001278929.1:p.Asn280Thr
NM_000171.4:c.1088A>C MANE Select	NP_000162.2:p.Asn363Thr
NM_001146040.2:c.1112A>C	NP_001139512.1:p.Asn371Thr
NM_001292000.2:c.839A>C	NP_001278929.1:p.Asn280Thr