Canonical Allele Identifier: CA129985880
Gene: GLRA1 HGNC NCBI

Linked Data

dbSNP Id: rs560210318

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151851279A>G , CM000667.2:g.151851279A>G GRCh38
NC_000005.9:g.151230840A>G , CM000667.1:g.151230840A>G GRCh37
NC_000005.8:g.151211033A>G NCBI36
NG_011764.1:g.78558T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.912+111T>C MANE Select ENSP00000274576.5:n.912+111T>C
ENST00000274576.8:c.912+111T>C ENSP00000274576.4:n.912+111T>C
ENST00000455880.2:c.912+111T>C ENSP00000411593.2:n.912+111T>C
ENST00000462581.6:c.*670+111T>C ENSP00000430595.1:n.*670+111T>C
ENST00000471351.2:n.1195+111T>C
NM_000171.3:c.912+111T>C NP_000162.2:n.912+111T>C
NM_001146040.1:c.912+111T>C NP_001139512.1:n.912+111T>C
NM_001292000.1:c.663+111T>C NP_001278929.1:n.663+111T>C
XM_005268412.2:c.912+111T>C XP_005268469.1:n.912+111T>C
NM_000171.4:c.912+111T>C MANE Select NP_000162.2:n.912+111T>C
NM_001146040.2:c.912+111T>C NP_001139512.1:n.912+111T>C
NM_001292000.2:c.663+111T>C NP_001278929.1:n.663+111T>C