Canonical Allele Identifier: CA361838026

Gene: GLRA1

Linked Data

• MyVariant Identifiers: chr5:g.151231112A>C (hg19) ; chr5:g.151851551A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151851551A>C , CM000667.2:g.151851551A>C	GRCh38
NC_000005.9:g.151231112A>C , CM000667.1:g.151231112A>C	GRCh37
NC_000005.8:g.151211305A>C	NCBI36
NG_011764.1:g.78286T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.751T>G MANE Select	ENSP00000274576.5:p.Tyr251Asp
ENST00000274576.8:c.751T>G	ENSP00000274576.4:p.Tyr251Asp
ENST00000455880.2:c.751T>G	ENSP00000411593.2:p.Tyr251Asp
ENST00000462581.6:c.*509T>G	ENSP00000430595.1:n.*509T>G
ENST00000471351.2:n.1034T>G
NM_000171.3:c.751T>G	NP_000162.2:p.Tyr251Asp
NM_001146040.1:c.751T>G	NP_001139512.1:p.Tyr251Asp
NM_001292000.1:c.502T>G	NP_001278929.1:p.Tyr168Asp
XM_005268412.2:c.751T>G	XP_005268469.1:p.Tyr251Asp
NM_000171.4:c.751T>G MANE Select	NP_000162.2:p.Tyr251Asp
NM_001146040.2:c.751T>G	NP_001139512.1:p.Tyr251Asp
NM_001292000.2:c.502T>G	NP_001278929.1:p.Tyr168Asp