Canonical Allele Identifier: CA986871641

Gene: GCGR

Linked Data

• dbSNP Id: rs2038049665
• gnomAD v3: 17-81809634-C-CTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT
• gnomAD v4: 17-81809634-C-CTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809634_81809635insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT , CM000679.2:g.81809634_81809635insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT	GRCh38
NC_000017.10:g.79767510_79767511insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT , CM000679.1:g.79767510_79767511insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT	GRCh37
NG_016409.1:g.8461_8462insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-148_61-147insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT MANE Select	ENSP00000383558.3:n.61-148_61-147insTGTCCGTCTGTCCATCTGCCTATCC...
ENST00000400723.7:c.61-148_61-147insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT	ENSP00000383558.3:n.61-148_61-147insTGTCCGTCTGTCCATCTGCCTATCC...
ENST00000570996.5:c.61-148_61-147insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT	ENSP00000460976.1:n.61-148_61-147insTGTCCGTCTGTCCATCTGCCTATCC...
ENST00000572185.1:n.356-148_356-147insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT
ENST00000573428.1:c.61-148_61-147insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT	ENSP00000458930.1:n.61-148_61-147insTGTCCGTCTGTCCATCTGCCTATCC...
NM_000160.4:c.61-148_61-147insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT	NP_000151.1:n.61-148_61-147insTGTCCGTCTGTCCATCTGCCTATCCATCTGC...
XM_006722277.1:c.61-148_61-147insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT	XP_006722340.1:n.61-148_61-147insTGTCCGTCTGTCCATCTGCCTATCCATC...
XM_011523539.1:c.-166-148_-166-147insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT	XP_011521841.1:n.-166-148_-166-147insTGTCCGTCTGTCCATCTGCCTATC...
XM_011523540.1:c.-456-148_-456-147insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT	XP_011521842.1:n.-456-148_-456-147insTGTCCGTCTGTCCATCTGCCTATC...
XM_017024446.1:c.61-154_61-153insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT	XP_016879935.1:n.61-154_61-153insTGTCCGTCTGTCCATCTGCCTATCCATC...
XM_017024447.1:c.-450-154_-450-153insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT	XP_016879936.1:n.-450-154_-450-153insTGTCCGTCTGTCCATCTGCCTATC...
NM_000160.5:c.61-148_61-147insTGTCCGTCTGTCCATCTGCCTATCCATCTGCCTGCCTATCTGT MANE Select	NP_000151.1:n.61-148_61-147insTGTCCGTCTGTCCATCTGCCTATCCATCTGC...