Canonical Allele Identifier: CA986871821

Gene: GCGR

Linked Data

• dbSNP Id: rs2038051350
• gnomAD v3: 17-81809677-ATCTGCCTATCCATCTACCTGCCTGCCTGTCTGCCTGTCTGTCTGCCTGTCTG-A
• gnomAD v4: 17-81809677-ATCTGCCTATCCATCTACCTGCCTGCCTGTCTGCCTGTCTGTCTGCCTGTCTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809685_81809736del , CM000679.2:g.81809685_81809736del	GRCh38
NC_000017.10:g.79767561_79767612del , CM000679.1:g.79767561_79767612del	GRCh37
NG_016409.1:g.8512_8563del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-97_61-46del MANE Select	ENSP00000383558.3:n.61-97_61-46del
ENST00000400723.7:c.61-97_61-46del	ENSP00000383558.3:n.61-97_61-46del
ENST00000570996.5:c.61-97_61-46del	ENSP00000460976.1:n.61-97_61-46del
ENST00000572185.1:n.356-97_356-46del
ENST00000573428.1:c.61-97_61-46del	ENSP00000458930.1:n.61-97_61-46del
NM_000160.4:c.61-97_61-46del	NP_000151.1:n.61-97_61-46del
XM_006722277.1:c.61-97_61-46del	XP_006722340.1:n.61-97_61-46del
XM_011523539.1:c.-166-97_-166-46del	XP_011521841.1:n.-166-97_-166-46del
XM_011523540.1:c.-456-97_-456-46del	XP_011521842.1:n.-456-97_-456-46del
XM_017024446.1:c.61-103_61-52del	XP_016879935.1:n.61-103_61-52del
XM_017024447.1:c.-450-103_-450-52del	XP_016879936.1:n.-450-103_-450-52del
NM_000160.5:c.61-97_61-46del MANE Select	NP_000151.1:n.61-97_61-46del