Canonical Allele Identifier: CA627768243

Gene: GCGR

Linked Data

• dbSNP Id: rs745907164
• gnomAD v2: 17-79767602-T-TCTGTCTGCCTGCCTGTCTGCCTGTCTGTCTGCCTGC
• gnomAD v3: 17-81809726-T-TCTGTCTGCCTGCCTGTCTGCCTGTCTGTCTGCCTGC
• gnomAD v4: 17-81809726-T-TCTGTCTGCCTGCCTGTCTGCCTGTCTGTCTGCCTGC
• MyVariant Identifiers: chr17:g.79767602_79767603insCTGTCTGCCTGCCTGTCTGCCTGTCTGTCTGCCTGC (hg19) ; chr17:g.81809726_81809727insCTGTCTGCCTGCCTGTCTGCCTGTCTGTCTGCCTGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809745_81809746insCCTGTCTGTCTGCCTGCCTGTCTGCCTGCCTGTCTG , CM000679.2:g.81809745_81809746insCCTGTCTGTCTGCCTGCCTGTCTGCCTGCCTGTCTG	GRCh38
NC_000017.10:g.79767621_79767622insCCTGTCTGTCTGCCTGCCTGTCTGCCTGCCTGTCTG , CM000679.1:g.79767621_79767622insCCTGTCTGTCTGCCTGCCTGTCTGCCTGCCTGTCTG	GRCh37
NG_016409.1:g.8572_8573insCCTGTCTGTCTGCCTGCCTGTCTGCCTGCCTGTCTG

Transcript Alleles

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