Canonical Allele Identifier: CA361852008

Gene: GLRA1

Linked Data

• MyVariant Identifiers: chr5:g.151829093_151829094del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151829094_151829095del , CM000667.2:g.151829094_151829095del	GRCh38
NC_000005.9:g.151208655_151208656del , CM000667.1:g.151208655_151208656del	GRCh37
NC_000005.8:g.151188848_151188849del	NCBI36
NG_011764.1:g.100743_100744del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.913-27_913-26del MANE Select	ENSP00000274576.5:n.913-27_913-26del
ENST00000274576.8:c.913-27_913-26del	ENSP00000274576.4:n.913-27_913-26del
ENST00000455880.2:c.913-27_913-26del	ENSP00000411593.2:n.913-27_913-26del
ENST00000462581.6:c.*671-27_*671-26del	ENSP00000430595.1:n.*671-27_*671-26del
NM_000171.3:c.913-27_913-26del	NP_000162.2:n.913-27_913-26del
NM_001146040.1:c.913-27_913-26del	NP_001139512.1:n.913-27_913-26del
NM_001292000.1:c.664-27_664-26del	NP_001278929.1:n.664-27_664-26del
NM_000171.4:c.913-27_913-26del MANE Select	NP_000162.2:n.913-27_913-26del
NM_001146040.2:c.913-27_913-26del	NP_001139512.1:n.913-27_913-26del
NM_001292000.2:c.664-27_664-26del	NP_001278929.1:n.664-27_664-26del