Canonical Allele Identifier: CA341369

Gene: GLRA1

Linked Data

• ClinVar Variation Id: 16066
• ClinVar RCV Id: RCV000017444
• dbSNP Id: rs121918413
• MyVariant Identifiers: chr5:g.151231031G>T (hg19) ; chr5:g.151851470G>T (hg38)
• PubMed: PMID:9920650 ; PMID:20301437

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151851470G>T , CM000667.2:g.151851470G>T	GRCh38
NC_000005.9:g.151231031G>T , CM000667.1:g.151231031G>T	GRCh37
NC_000005.8:g.151211224G>T	NCBI36
NG_011764.1:g.78367C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.832C>A MANE Select	ENSP00000274576.5:p.Pro278Thr
ENST00000274576.8:c.832C>A	ENSP00000274576.4:p.Pro278Thr
ENST00000455880.2:c.832C>A	ENSP00000411593.2:p.Pro278Thr
ENST00000462581.6:c.*590C>A	ENSP00000430595.1:n.*590C>A
ENST00000471351.2:n.1115C>A
NM_000171.3:c.832C>A	NP_000162.2:p.Pro278Thr
NM_001146040.1:c.832C>A	NP_001139512.1:p.Pro278Thr
NM_001292000.1:c.583C>A	NP_001278929.1:p.Pro195Thr
XM_005268412.2:c.832C>A	XP_005268469.1:p.Pro278Thr
NM_000171.4:c.832C>A MANE Select	NP_000162.2:p.Pro278Thr
NM_001146040.2:c.832C>A	NP_001139512.1:p.Pro278Thr
NM_001292000.2:c.583C>A	NP_001278929.1:p.Pro195Thr