Canonical Allele Identifier: CA1591565380
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151823085_151823086delinsAT , CM000667.2:g.151823085_151823086delinsAT GRCh38
NC_000005.9:g.151202646_151202647delinsAT , CM000667.1:g.151202646_151202647delinsAT GRCh37
NC_000005.8:g.151182839_151182840delinsAT NCBI36
NG_011764.1:g.106751_106752delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.1060-123_1060-122delinsAT MANE Select ENSP00000274576.5:n.1060-123_1060-122delinsAT
ENST00000274576.8:c.1060-123_1060-122delinsAT ENSP00000274576.4:n.1060-123_1060-122delinsAT
ENST00000455880.2:c.1060-99_1060-98delinsAT ENSP00000411593.2:n.1060-99_1060-98delinsAT
ENST00000462581.6:c.*818-123_*818-122delinsAT ENSP00000430595.1:n.*818-123_*818-122delinsAT
NM_000171.3:c.1060-123_1060-122delinsAT NP_000162.2:n.1060-123_1060-122delinsAT
NM_001146040.1:c.1060-99_1060-98delinsAT NP_001139512.1:n.1060-99_1060-98delinsAT
NM_001292000.1:c.811-123_811-122delinsAT NP_001278929.1:n.811-123_811-122delinsAT
NM_000171.4:c.1060-123_1060-122delinsAT MANE Select NP_000162.2:n.1060-123_1060-122delinsAT
NM_001146040.2:c.1060-99_1060-98delinsAT NP_001139512.1:n.1060-99_1060-98delinsAT
NM_001292000.2:c.811-123_811-122delinsAT NP_001278929.1:n.811-123_811-122delinsAT