Canonical Allele Identifier: CA130011621

Gene: GLRA1

Linked Data

• dbSNP Id: rs547521465
• MyVariant Identifiers: chr5:g.151271825T>G (hg19) ; chr5:g.151892264T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151892264T>G , CM000667.2:g.151892264T>G	GRCh38
NC_000005.9:g.151271825T>G , CM000667.1:g.151271825T>G	GRCh37
NC_000005.8:g.151252018T>G	NCBI36
NG_011764.1:g.37573A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000274576.9:c.184+47A>C MANE Select	ENSP00000274576.5:n.184+47A>C
ENST00000274576.8:c.184+47A>C	ENSP00000274576.4:n.184+47A>C
ENST00000455880.2:c.184+47A>C	ENSP00000411593.2:n.184+47A>C
ENST00000462581.6:c.57-5476A>C	ENSP00000430595.1:n.57-5476A>C
ENST00000471351.2:n.467+47A>C
NM_000171.3:c.184+47A>C	NP_000162.2:n.184+47A>C
NM_001146040.1:c.184+47A>C	NP_001139512.1:n.184+47A>C
NM_001292000.1:c.-65-5476A>C	NP_001278929.1:n.-65-5476A>C
XM_005268412.2:c.184+47A>C	XP_005268469.1:n.184+47A>C
XR_002956230.1:n.3168T>G
NM_000171.4:c.184+47A>C MANE Select	NP_000162.2:n.184+47A>C
NM_001146040.2:c.184+47A>C	NP_001139512.1:n.184+47A>C
NM_001292000.2:c.-65-5476A>C	NP_001278929.1:n.-65-5476A>C