Canonical Allele Identifier: CA2576426167

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809745_81809746insCCAGCCTGTCTG , CM000679.2:g.81809745_81809746insCCAGCCTGTCTG	GRCh38
NC_000017.10:g.79767621_79767622insCCAGCCTGTCTG , CM000679.1:g.79767621_79767622insCCAGCCTGTCTG	GRCh37
NG_016409.1:g.8572_8573insCCAGCCTGTCTG

Transcript Alleles

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