Canonical Allele Identifier: CA2676110983

Gene: GLRA1

Linked Data

• gnomAD v4: 5-151851609-A-ATTG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151851609_151851610insTTG , CM000667.2:g.151851609_151851610insTTG	GRCh38
NC_000005.9:g.151231170_151231171insTTG , CM000667.1:g.151231170_151231171insTTG	GRCh37
NC_000005.8:g.151211363_151211364insTTG	NCBI36
NG_011764.1:g.78227_78228insCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.698-6_698-5insCAA MANE Select	ENSP00000274576.5:n.698-6_698-5insCAA
ENST00000274576.8:c.698-6_698-5insCAA	ENSP00000274576.4:n.698-6_698-5insCAA
ENST00000455880.2:c.698-6_698-5insCAA	ENSP00000411593.2:n.698-6_698-5insCAA
ENST00000462581.6:c.*456-6_*456-5insCAA	ENSP00000430595.1:n.*456-6_*456-5insCAA
ENST00000471351.2:n.981-6_981-5insCAA
NM_000171.3:c.698-6_698-5insCAA	NP_000162.2:n.698-6_698-5insCAA
NM_001146040.1:c.698-6_698-5insCAA	NP_001139512.1:n.698-6_698-5insCAA
NM_001292000.1:c.449-6_449-5insCAA	NP_001278929.1:n.449-6_449-5insCAA
XM_005268412.2:c.698-6_698-5insCAA	XP_005268469.1:n.698-6_698-5insCAA
NM_000171.4:c.698-6_698-5insCAA MANE Select	NP_000162.2:n.698-6_698-5insCAA
NM_001146040.2:c.698-6_698-5insCAA	NP_001139512.1:n.698-6_698-5insCAA
NM_001292000.2:c.449-6_449-5insCAA	NP_001278929.1:n.449-6_449-5insCAA