Canonical Allele Identifier: CA986871951

Gene: GCGR

Linked Data

• gnomAD v3: 17-81809729-G-GTCCGTCTGTCCATCTGCCTATCCA
• gnomAD v4: 17-81809729-G-GTCCGTCTGTCCATCTGCCTATCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809731_81809732insCGTCTGTCCATCTGCCTATCCATC , CM000679.2:g.81809731_81809732insCGTCTGTCCATCTGCCTATCCATC	GRCh38
NC_000017.10:g.79767607_79767608insCGTCTGTCCATCTGCCTATCCATC , CM000679.1:g.79767607_79767608insCGTCTGTCCATCTGCCTATCCATC	GRCh37
NG_016409.1:g.8558_8559insCGTCTGTCCATCTGCCTATCCATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-51_61-50insCGTCTGTCCATCTGCCTATCCATC MANE Select	ENSP00000383558.3:n.61-51_61-50insCGTCTGTCCATCTGCCTATCCATC
ENST00000400723.7:c.61-51_61-50insCGTCTGTCCATCTGCCTATCCATC	ENSP00000383558.3:n.61-51_61-50insCGTCTGTCCATCTGCCTATCCATC
ENST00000570996.5:c.61-51_61-50insCGTCTGTCCATCTGCCTATCCATC	ENSP00000460976.1:n.61-51_61-50insCGTCTGTCCATCTGCCTATCCATC
ENST00000572185.1:n.356-51_356-50insCGTCTGTCCATCTGCCTATCCATC
ENST00000573428.1:c.61-51_61-50insCGTCTGTCCATCTGCCTATCCATC	ENSP00000458930.1:n.61-51_61-50insCGTCTGTCCATCTGCCTATCCATC
NM_000160.4:c.61-51_61-50insCGTCTGTCCATCTGCCTATCCATC	NP_000151.1:n.61-51_61-50insCGTCTGTCCATCTGCCTATCCATC
XM_006722277.1:c.61-51_61-50insCGTCTGTCCATCTGCCTATCCATC	XP_006722340.1:n.61-51_61-50insCGTCTGTCCATCTGCCTATCCATC
XM_011523539.1:c.-166-51_-166-50insCGTCTGTCCATCTGCCTATCCATC	XP_011521841.1:n.-166-51_-166-50insCGTCTGTCCATCTGCCTATCCATC
XM_011523540.1:c.-456-51_-456-50insCGTCTGTCCATCTGCCTATCCATC	XP_011521842.1:n.-456-51_-456-50insCGTCTGTCCATCTGCCTATCCATC
XM_017024446.1:c.61-57_61-56insCGTCTGTCCATCTGCCTATCCATC	XP_016879935.1:n.61-57_61-56insCGTCTGTCCATCTGCCTATCCATC
XM_017024447.1:c.-450-57_-450-56insCGTCTGTCCATCTGCCTATCCATC	XP_016879936.1:n.-450-57_-450-56insCGTCTGTCCATCTGCCTATCCATC
NM_000160.5:c.61-51_61-50insCGTCTGTCCATCTGCCTATCCATC MANE Select	NP_000151.1:n.61-51_61-50insCGTCTGTCCATCTGCCTATCCATC