Canonical Allele Identifier: CA361841173
Gene: GLRA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151859794T>G , CM000667.2:g.151859794T>G GRCh38
NC_000005.9:g.151239355T>G , CM000667.1:g.151239355T>G GRCh37
NC_000005.8:g.151219548T>G NCBI36
NG_011764.1:g.70043A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000274576.9:c.467A>C MANE Select ENSP00000274576.5:p.Tyr156Ser
ENST00000274576.8:c.467A>C ENSP00000274576.4:p.Tyr156Ser
ENST00000455880.2:c.467A>C ENSP00000411593.2:p.Tyr156Ser
ENST00000462581.6:c.*225A>C ENSP00000430595.1:n.*225A>C
ENST00000471351.2:n.750A>C
NM_000171.3:c.467A>C NP_000162.2:p.Tyr156Ser
NM_001146040.1:c.467A>C NP_001139512.1:p.Tyr156Ser
NM_001292000.1:c.218A>C NP_001278929.1:p.Tyr73Ser
XM_005268412.2:c.467A>C XP_005268469.1:p.Tyr156Ser
XR_002956230.1:n.229+1901T>G
NM_000171.4:c.467A>C MANE Select NP_000162.2:p.Tyr156Ser
NM_001146040.2:c.467A>C NP_001139512.1:p.Tyr156Ser
NM_001292000.2:c.218A>C NP_001278929.1:p.Tyr73Ser