Canonical Allele Identifier: CA2278679864

Gene: GCGR

Linked Data

• dbSNP Id: rs1440874293
• gnomAD v4: 17-81809669-G-GTCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809671_81809672insCATC , CM000679.2:g.81809671_81809672insCATC	GRCh38
NC_000017.10:g.79767547_79767548insCATC , CM000679.1:g.79767547_79767548insCATC	GRCh37
NG_016409.1:g.8498_8499insCATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-111_61-110insCATC MANE Select	ENSP00000383558.3:n.61-111_61-110insCATC
ENST00000400723.7:c.61-111_61-110insCATC	ENSP00000383558.3:n.61-111_61-110insCATC
ENST00000570996.5:c.61-111_61-110insCATC	ENSP00000460976.1:n.61-111_61-110insCATC
ENST00000572185.1:n.356-111_356-110insCATC
ENST00000573428.1:c.61-111_61-110insCATC	ENSP00000458930.1:n.61-111_61-110insCATC
NM_000160.4:c.61-111_61-110insCATC	NP_000151.1:n.61-111_61-110insCATC
XM_006722277.1:c.61-111_61-110insCATC	XP_006722340.1:n.61-111_61-110insCATC
XM_011523539.1:c.-166-111_-166-110insCATC	XP_011521841.1:n.-166-111_-166-110insCATC
XM_011523540.1:c.-456-111_-456-110insCATC	XP_011521842.1:n.-456-111_-456-110insCATC
XM_017024446.1:c.61-117_61-116insCATC	XP_016879935.1:n.61-117_61-116insCATC
XM_017024447.1:c.-450-117_-450-116insCATC	XP_016879936.1:n.-450-117_-450-116insCATC
NM_000160.5:c.61-111_61-110insCATC MANE Select	NP_000151.1:n.61-111_61-110insCATC