Canonical Allele Identifier: CA1591596145
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151892266T= , CM000667.2:g.151892266T= GRCh38
NC_000005.9:g.151271827T= , CM000667.1:g.151271827T= GRCh37
NC_000005.8:g.151252020T= NCBI36
NG_011764.1:g.37571A=

Transcript Alleles

HGVS Amino-acid change
ENST00000274576.9:c.184+45A= MANE Select ENSP00000274576.5:n.184+45A=
ENST00000274576.8:c.184+45A= ENSP00000274576.4:n.184+45A=
ENST00000455880.2:c.184+45A= ENSP00000411593.2:n.184+45A=
ENST00000462581.6:c.57-5478A= ENSP00000430595.1:n.57-5478A=
ENST00000471351.2:n.467+45A=
NM_000171.3:c.184+45A= NP_000162.2:n.184+45A=
NM_001146040.1:c.184+45A= NP_001139512.1:n.184+45A=
NM_001292000.1:c.-65-5478A= NP_001278929.1:n.-65-5478A=
XM_005268412.2:c.184+45A= XP_005268469.1:n.184+45A=
XR_002956230.1:n.3170T=
NM_000171.4:c.184+45A= MANE Select NP_000162.2:n.184+45A=
NM_001146040.2:c.184+45A= NP_001139512.1:n.184+45A=
NM_001292000.2:c.-65-5478A= NP_001278929.1:n.-65-5478A=