Canonical Allele Identifier: CA361837642

Gene: GLRA1

Linked Data

• MyVariant Identifiers: chr5:g.151231039T>A (hg19) ; chr5:g.151851478T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151851478T>A , CM000667.2:g.151851478T>A	GRCh38
NC_000005.9:g.151231039T>A , CM000667.1:g.151231039T>A	GRCh37
NC_000005.8:g.151211232T>A	NCBI36
NG_011764.1:g.78359A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.824A>T MANE Select	ENSP00000274576.5:p.Asp275Val
ENST00000274576.8:c.824A>T	ENSP00000274576.4:p.Asp275Val
ENST00000455880.2:c.824A>T	ENSP00000411593.2:p.Asp275Val
ENST00000462581.6:c.*582A>T	ENSP00000430595.1:n.*582A>T
ENST00000471351.2:n.1107A>T
NM_000171.3:c.824A>T	NP_000162.2:p.Asp275Val
NM_001146040.1:c.824A>T	NP_001139512.1:p.Asp275Val
NM_001292000.1:c.575A>T	NP_001278929.1:p.Asp192Val
XM_005268412.2:c.824A>T	XP_005268469.1:p.Asp275Val
NM_000171.4:c.824A>T MANE Select	NP_000162.2:p.Asp275Val
NM_001146040.2:c.824A>T	NP_001139512.1:p.Asp275Val
NM_001292000.2:c.575A>T	NP_001278929.1:p.Asp192Val