Canonical Allele Identifier: CA361849708

Gene: GLRA1

Linked Data

• gnomAD v4: 5-151822718-C-T
• MyVariant Identifiers: chr5:g.151202279C>T (hg19) ; chr5:g.151822718C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151822718C>T , CM000667.2:g.151822718C>T	GRCh38
NC_000005.9:g.151202279C>T , CM000667.1:g.151202279C>T	GRCh37
NC_000005.8:g.151182472C>T	NCBI36
NG_011764.1:g.107119G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.1305G>A MANE Select	ENSP00000274576.5:p.Trp435Ter
ENST00000274576.8:c.1305G>A	ENSP00000274576.4:p.Trp435Ter
ENST00000455880.2:c.1329G>A	ENSP00000411593.2:p.Trp443Ter
ENST00000462581.6:c.*1063G>A	ENSP00000430595.1:n.*1063G>A
NM_000171.3:c.1305G>A	NP_000162.2:p.Trp435Ter
NM_001146040.1:c.1329G>A	NP_001139512.1:p.Trp443Ter
NM_001292000.1:c.1056G>A	NP_001278929.1:p.Trp352Ter
NM_000171.4:c.1305G>A MANE Select	NP_000162.2:p.Trp435Ter
NM_001146040.2:c.1329G>A	NP_001139512.1:p.Trp443Ter
NM_001292000.2:c.1056G>A	NP_001278929.1:p.Trp352Ter