Canonical Allele Identifier: CA361842127

Gene: GLRA1

Linked Data

• MyVariant Identifiers: chr5:g.151239532T>G (hg19) ; chr5:g.151859971T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151859971T>G , CM000667.2:g.151859971T>G	GRCh38
NC_000005.9:g.151239532T>G , CM000667.1:g.151239532T>G	GRCh37
NC_000005.8:g.151219725T>G	NCBI36
NG_011764.1:g.69866A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000274576.9:c.290A>C MANE Select	ENSP00000274576.5:p.Asn97Thr
ENST00000274576.8:c.290A>C	ENSP00000274576.4:p.Asn97Thr
ENST00000455880.2:c.290A>C	ENSP00000411593.2:p.Asn97Thr
ENST00000462581.6:c.*48A>C	ENSP00000430595.1:n.*48A>C
ENST00000471351.2:n.573A>C
NM_000171.3:c.290A>C	NP_000162.2:p.Asn97Thr
NM_001146040.1:c.290A>C	NP_001139512.1:p.Asn97Thr
NM_001292000.1:c.41A>C	NP_001278929.1:p.Asn14Thr
XM_005268412.2:c.290A>C	XP_005268469.1:p.Asn97Thr
XR_002956230.1:n.229+2078T>G
NM_000171.4:c.290A>C MANE Select	NP_000162.2:p.Asn97Thr
NM_001146040.2:c.290A>C	NP_001139512.1:p.Asn97Thr
NM_001292000.2:c.41A>C	NP_001278929.1:p.Asn14Thr