Canonical Allele Identifier: CA555974114

Gene: GLRB

Linked Data

• dbSNP Id: rs1365050773
• gnomAD v2: 4-158057942-A-AT
• gnomAD v4: 4-157136790-A-AT
• MyVariant Identifiers: chr4:g.158057942_158057943insT (hg19) ; chr4:g.157136790_157136791insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.157136793dup , CM000666.2:g.157136793dup	GRCh38
NC_000004.11:g.158057945dup , CM000666.1:g.158057945dup	GRCh37
NC_000004.10:g.158277395dup	NCBI36
NG_015823.1:g.65669dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264428.9:c.528-11dup MANE Select	ENSP00000264428.4:n.528-11dup
ENST00000264428.8:c.528-11dup	ENSP00000264428.4:n.528-11dup
ENST00000506411.5:c.*448-11dup	ENSP00000422039.1:n.*448-11dup
ENST00000509282.1:c.528-11dup	ENSP00000427186.1:n.528-11dup
ENST00000510970.1:n.335-11dup
ENST00000512619.5:c.123-33639dup	ENSP00000425433.1:n.123-33639dup
ENST00000541722.5:c.528-11dup	ENSP00000441873.1:n.528-11dup
NM_000824.4:c.528-11dup	NP_000815.1:n.528-11dup
NM_001166060.1:c.528-11dup	NP_001159532.1:n.528-11dup
NM_001166061.1:c.528-11dup	NP_001159533.1:n.528-11dup
XM_011531876.1:c.234-11dup	XP_011530178.1:n.234-11dup
XM_017008034.1:c.234-11dup	XP_016863523.1:n.234-11dup
XM_017008035.2:c.528-11dup	XP_016863524.1:n.528-11dup
XR_001741207.2:n.709-11dup
XR_002959723.1:n.709-11dup
NM_000824.5:c.528-11dup MANE Select	NP_000815.1:n.528-11dup
NM_001166060.2:c.528-11dup	NP_001159532.1:n.528-11dup
NM_001166061.2:c.528-11dup	NP_001159533.1:n.528-11dup