Canonical Allele Identifier: CA1591595994
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151892449_151892454delinsAGAGAG , CM000667.2:g.151892449_151892454delinsAGAGAG GRCh38
NC_000005.9:g.151272010_151272015delinsAGAGAG , CM000667.1:g.151272010_151272015delinsAGAGAG GRCh37
NC_000005.8:g.151252203_151252208delinsAGAGAG NCBI36
NG_011764.1:g.37383_37388delinsCTCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.57-16_57-11delinsCTCTCT MANE Select ENSP00000274576.5:n.57-16_57-11delinsCTCTCT
ENST00000274576.8:c.57-16_57-11delinsCTCTCT ENSP00000274576.4:n.57-16_57-11delinsCTCTCT
ENST00000455880.2:c.57-16_57-11delinsCTCTCT ENSP00000411593.2:n.57-16_57-11delinsCTCTCT
ENST00000462581.6:c.57-5666_57-5661delinsCTCTCT ENSP00000430595.1:n.57-5666_57-5661delinsCTCTCT
ENST00000471351.2:n.340-16_340-11delinsCTCTCT
NM_000171.3:c.57-16_57-11delinsCTCTCT NP_000162.2:n.57-16_57-11delinsCTCTCT
NM_001146040.1:c.57-16_57-11delinsCTCTCT NP_001139512.1:n.57-16_57-11delinsCTCTCT
NM_001292000.1:c.-65-5666_-65-5661delinsCTCTCT NP_001278929.1:n.-65-5666_-65-5661delinsCTCTCT
XM_005268412.2:c.57-16_57-11delinsCTCTCT XP_005268469.1:n.57-16_57-11delinsCTCTCT
NM_000171.4:c.57-16_57-11delinsCTCTCT MANE Select NP_000162.2:n.57-16_57-11delinsCTCTCT
NM_001146040.2:c.57-16_57-11delinsCTCTCT NP_001139512.1:n.57-16_57-11delinsCTCTCT
NM_001292000.2:c.-65-5666_-65-5661delinsCTCTCT NP_001278929.1:n.-65-5666_-65-5661delinsCTCTCT