Canonical Allele Identifier: CA130005978

Gene: GLRA1

Linked Data

• dbSNP Id: rs890814369
• gnomAD v3: 5-151822611-C-T
• gnomAD v4: 5-151822611-C-T
• MyVariant Identifiers: chr5:g.151202172C>T (hg19) ; chr5:g.151822611C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151822611C>T , CM000667.2:g.151822611C>T	GRCh38
NC_000005.9:g.151202172C>T , CM000667.1:g.151202172C>T	GRCh37
NC_000005.8:g.151182365C>T	NCBI36
NG_011764.1:g.107226G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.*62G>A MANE Select	ENSP00000274576.5:n.*62G>A
ENST00000274576.8:c.*62G>A	ENSP00000274576.4:n.*62G>A
NM_000171.3:c.*62G>A	NP_000162.2:n.*62G>A
NM_001146040.1:c.*62G>A	NP_001139512.1:n.*62G>A
NM_001292000.1:c.*62G>A	NP_001278929.1:n.*62G>A
NM_000171.4:c.*62G>A MANE Select	NP_000162.2:n.*62G>A
NM_001146040.2:c.*62G>A	NP_001139512.1:n.*62G>A
NM_001292000.2:c.*62G>A	NP_001278929.1:n.*62G>A