Canonical Allele Identifier: CA361847961
Gene: GLRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1328520178

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151892365T>A , CM000667.2:g.151892365T>A GRCh38
NC_000005.9:g.151271926T>A , CM000667.1:g.151271926T>A GRCh37
NC_000005.8:g.151252119T>A NCBI36
NG_011764.1:g.37472A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274576.9:c.130A>T MANE Select ENSP00000274576.5:p.Lys44Ter
ENST00000274576.8:c.130A>T ENSP00000274576.4:p.Lys44Ter
ENST00000455880.2:c.130A>T ENSP00000411593.2:p.Lys44Ter
ENST00000462581.6:c.57-5577A>T ENSP00000430595.1:n.57-5577A>T
ENST00000471351.2:n.413A>T
NM_000171.3:c.130A>T NP_000162.2:p.Lys44Ter
NM_001146040.1:c.130A>T NP_001139512.1:p.Lys44Ter
NM_001292000.1:c.-65-5577A>T NP_001278929.1:n.-65-5577A>T
XM_005268412.2:c.130A>T XP_005268469.1:p.Lys44Ter
XR_002956230.1:n.3269T>A
NM_000171.4:c.130A>T MANE Select NP_000162.2:p.Lys44Ter
NM_001146040.2:c.130A>T NP_001139512.1:p.Lys44Ter
NM_001292000.2:c.-65-5577A>T NP_001278929.1:n.-65-5577A>T