Canonical Allele Identifier: CA2768928666
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151823054_151823060del , CM000667.2:g.151823054_151823060del GRCh38
NC_000005.9:g.151202615_151202621del , CM000667.1:g.151202615_151202621del GRCh37
NC_000005.8:g.151182808_151182814del NCBI36
NG_011764.1:g.106777_106783del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.1060-97_1060-91del MANE Select ENSP00000274576.5:n.1060-97_1060-91del
ENST00000274576.8:c.1060-97_1060-91del ENSP00000274576.4:n.1060-97_1060-91del
ENST00000455880.2:c.1060-73_1060-67del ENSP00000411593.2:n.1060-73_1060-67del
ENST00000462581.6:c.*818-97_*818-91del ENSP00000430595.1:n.*818-97_*818-91del
NM_000171.3:c.1060-97_1060-91del NP_000162.2:n.1060-97_1060-91del
NM_001146040.1:c.1060-73_1060-67del NP_001139512.1:n.1060-73_1060-67del
NM_001292000.1:c.811-97_811-91del NP_001278929.1:n.811-97_811-91del
NM_000171.4:c.1060-97_1060-91del MANE Select NP_000162.2:n.1060-97_1060-91del
NM_001146040.2:c.1060-73_1060-67del NP_001139512.1:n.1060-73_1060-67del
NM_001292000.2:c.811-97_811-91del NP_001278929.1:n.811-97_811-91del