Canonical Allele Identifier: CA2672486547

Gene: GLRB

Linked Data

• gnomAD v4: 4-157136710-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.157136710_157136711insGG , CM000666.2:g.157136710_157136711insGG	GRCh38
NC_000004.11:g.158057862_158057863insGG , CM000666.1:g.158057862_158057863insGG	GRCh37
NC_000004.10:g.158277312_158277313insGG	NCBI36
NG_015823.1:g.65586_65587insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264428.9:c.527+12_527+13insGG MANE Select	ENSP00000264428.4:n.527+12_527+13insGG
ENST00000264428.8:c.527+12_527+13insGG	ENSP00000264428.4:n.527+12_527+13insGG
ENST00000506411.5:c.*447+12_*447+13insGG	ENSP00000422039.1:n.*447+12_*447+13insGG
ENST00000509282.1:c.527+12_527+13insGG	ENSP00000427186.1:n.527+12_527+13insGG
ENST00000510970.1:n.334+12_334+13insGG
ENST00000512619.5:c.123-33722_123-33721insGG	ENSP00000425433.1:n.123-33722_123-33721insGG
ENST00000541722.5:c.527+12_527+13insGG	ENSP00000441873.1:n.527+12_527+13insGG
NM_000824.4:c.527+12_527+13insGG	NP_000815.1:n.527+12_527+13insGG
NM_001166060.1:c.527+12_527+13insGG	NP_001159532.1:n.527+12_527+13insGG
NM_001166061.1:c.527+12_527+13insGG	NP_001159533.1:n.527+12_527+13insGG
XM_011531876.1:c.233+12_233+13insGG	XP_011530178.1:n.233+12_233+13insGG
XM_017008034.1:c.233+12_233+13insGG	XP_016863523.1:n.233+12_233+13insGG
XM_017008035.2:c.527+12_527+13insGG	XP_016863524.1:n.527+12_527+13insGG
XR_001741207.2:n.708+12_708+13insGG
XR_002959723.1:n.708+12_708+13insGG
NM_000824.5:c.527+12_527+13insGG MANE Select	NP_000815.1:n.527+12_527+13insGG
NM_001166060.2:c.527+12_527+13insGG	NP_001159532.1:n.527+12_527+13insGG
NM_001166061.2:c.527+12_527+13insGG	NP_001159533.1:n.527+12_527+13insGG