Canonical Allele Identifier: CA8841989

Gene: GCGR

Linked Data

• dbSNP Id: rs761305271
• ExAC: 17:79767621 G / GCC
• gnomAD v2: 17-79767621-G-GCC
• gnomAD v3: 17-81809745-G-GCC
• gnomAD v4: 17-81809745-G-GCC
• MyVariant Identifiers: chr17:g.79767621_79767622insCC (hg19) ; chr17:g.81809745_81809746insCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809745_81809746insCC , CM000679.2:g.81809745_81809746insCC	GRCh38
NC_000017.10:g.79767621_79767622insCC , CM000679.1:g.79767621_79767622insCC	GRCh37
NG_016409.1:g.8572_8573insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-37_61-36insCC MANE Select	ENSP00000383558.3:n.61-37_61-36insCC
ENST00000400723.7:c.61-37_61-36insCC	ENSP00000383558.3:n.61-37_61-36insCC
ENST00000570996.5:c.61-37_61-36insCC	ENSP00000460976.1:n.61-37_61-36insCC
ENST00000572185.1:n.356-37_356-36insCC
ENST00000573428.1:c.61-37_61-36insCC	ENSP00000458930.1:n.61-37_61-36insCC
NM_000160.4:c.61-37_61-36insCC	NP_000151.1:n.61-37_61-36insCC
XM_006722277.1:c.61-37_61-36insCC	XP_006722340.1:n.61-37_61-36insCC
XM_011523539.1:c.-166-37_-166-36insCC	XP_011521841.1:n.-166-37_-166-36insCC
XM_011523540.1:c.-456-37_-456-36insCC	XP_011521842.1:n.-456-37_-456-36insCC
XM_017024446.1:c.61-43_61-42insCC	XP_016879935.1:n.61-43_61-42insCC
XM_017024447.1:c.-450-43_-450-42insCC	XP_016879936.1:n.-450-43_-450-42insCC
NM_000160.5:c.61-37_61-36insCC MANE Select	NP_000151.1:n.61-37_61-36insCC