Canonical Allele Identifier: CA361841138

Gene: GLRA1

Linked Data

• MyVariant Identifiers: chr5:g.151239346C>G (hg19) ; chr5:g.151859785C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151859785C>G , CM000667.2:g.151859785C>G	GRCh38
NC_000005.9:g.151239346C>G , CM000667.1:g.151239346C>G	GRCh37
NC_000005.8:g.151219539C>G	NCBI36
NG_011764.1:g.70052G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.476G>C MANE Select	ENSP00000274576.5:p.Arg159Thr
ENST00000274576.8:c.476G>C	ENSP00000274576.4:p.Arg159Thr
ENST00000455880.2:c.476G>C	ENSP00000411593.2:p.Arg159Thr
ENST00000462581.6:c.*234G>C	ENSP00000430595.1:n.*234G>C
ENST00000471351.2:n.759G>C
NM_000171.3:c.476G>C	NP_000162.2:p.Arg159Thr
NM_001146040.1:c.476G>C	NP_001139512.1:p.Arg159Thr
NM_001292000.1:c.227G>C	NP_001278929.1:p.Arg76Thr
XM_005268412.2:c.476G>C	XP_005268469.1:p.Arg159Thr
XR_002956230.1:n.229+1892C>G
NM_000171.4:c.476G>C MANE Select	NP_000162.2:p.Arg159Thr
NM_001146040.2:c.476G>C	NP_001139512.1:p.Arg159Thr
NM_001292000.2:c.227G>C	NP_001278929.1:p.Arg76Thr