Canonical Allele Identifier: CA563631829

Gene: GLRA1

Linked Data

• dbSNP Id: rs1484908912
• gnomAD v2: 5-151231168-G-A
• gnomAD v4: 5-151851607-G-A
• MyVariant Identifiers: chr5:g.151231168G>A (hg19) ; chr5:g.151851607G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151851607G>A , CM000667.2:g.151851607G>A	GRCh38
NC_000005.9:g.151231168G>A , CM000667.1:g.151231168G>A	GRCh37
NC_000005.8:g.151211361G>A	NCBI36
NG_011764.1:g.78230C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.698-3C>T MANE Select	ENSP00000274576.5:n.698-3C>T
ENST00000274576.8:c.698-3C>T	ENSP00000274576.4:n.698-3C>T
ENST00000455880.2:c.698-3C>T	ENSP00000411593.2:n.698-3C>T
ENST00000462581.6:c.*456-3C>T	ENSP00000430595.1:n.*456-3C>T
ENST00000471351.2:n.981-3C>T
NM_000171.3:c.698-3C>T	NP_000162.2:n.698-3C>T
NM_001146040.1:c.698-3C>T	NP_001139512.1:n.698-3C>T
NM_001292000.1:c.449-3C>T	NP_001278929.1:n.449-3C>T
XM_005268412.2:c.698-3C>T	XP_005268469.1:n.698-3C>T
NM_000171.4:c.698-3C>T MANE Select	NP_000162.2:n.698-3C>T
NM_001146040.2:c.698-3C>T	NP_001139512.1:n.698-3C>T
NM_001292000.2:c.449-3C>T	NP_001278929.1:n.449-3C>T