Canonical Allele Identifier: CA2676110991

Gene: GLRA1

Linked Data

• gnomAD v4: 5-151851621-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151851624_151851625del , CM000667.2:g.151851624_151851625del	GRCh38
NC_000005.9:g.151231185_151231186del , CM000667.1:g.151231185_151231186del	GRCh37
NC_000005.8:g.151211378_151211379del	NCBI36
NG_011764.1:g.78214_78215del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.698-19_698-18del MANE Select	ENSP00000274576.5:n.698-19_698-18del
ENST00000274576.8:c.698-19_698-18del	ENSP00000274576.4:n.698-19_698-18del
ENST00000455880.2:c.698-19_698-18del	ENSP00000411593.2:n.698-19_698-18del
ENST00000462581.6:c.*456-19_*456-18del	ENSP00000430595.1:n.*456-19_*456-18del
ENST00000471351.2:n.981-19_981-18del
NM_000171.3:c.698-19_698-18del	NP_000162.2:n.698-19_698-18del
NM_001146040.1:c.698-19_698-18del	NP_001139512.1:n.698-19_698-18del
NM_001292000.1:c.449-19_449-18del	NP_001278929.1:n.449-19_449-18del
XM_005268412.2:c.698-19_698-18del	XP_005268469.1:n.698-19_698-18del
NM_000171.4:c.698-19_698-18del MANE Select	NP_000162.2:n.698-19_698-18del
NM_001146040.2:c.698-19_698-18del	NP_001139512.1:n.698-19_698-18del
NM_001292000.2:c.449-19_449-18del	NP_001278929.1:n.449-19_449-18del