Canonical Allele Identifier: CA627768200

Gene: GCGR

Linked Data

• dbSNP Id: rs1157570877
• gnomAD v2: 17-79767514-TCTGTCTGC-T
• gnomAD v3: 17-81809638-TCTGTCTGC-T
• gnomAD v4: 17-81809638-TCTGTCTGC-T
• MyVariant Identifiers: chr17:g.79767515_79767522del (hg19) ; chr17:g.81809639_81809646del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809654_81809661del , CM000679.2:g.81809654_81809661del	GRCh38
NC_000017.10:g.79767530_79767537del , CM000679.1:g.79767530_79767537del	GRCh37
NG_016409.1:g.8481_8488del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-128_61-121del MANE Select	ENSP00000383558.3:n.61-128_61-121del
ENST00000400723.7:c.61-128_61-121del	ENSP00000383558.3:n.61-128_61-121del
ENST00000570996.5:c.61-128_61-121del	ENSP00000460976.1:n.61-128_61-121del
ENST00000572185.1:n.356-128_356-121del
ENST00000573428.1:c.61-128_61-121del	ENSP00000458930.1:n.61-128_61-121del
NM_000160.4:c.61-128_61-121del	NP_000151.1:n.61-128_61-121del
XM_006722277.1:c.61-128_61-121del	XP_006722340.1:n.61-128_61-121del
XM_011523539.1:c.-166-128_-166-121del	XP_011521841.1:n.-166-128_-166-121del
XM_011523540.1:c.-456-128_-456-121del	XP_011521842.1:n.-456-128_-456-121del
XM_017024446.1:c.61-134_61-127del	XP_016879935.1:n.61-134_61-127del
XM_017024447.1:c.-450-134_-450-127del	XP_016879936.1:n.-450-134_-450-127del
NM_000160.5:c.61-128_61-121del MANE Select	NP_000151.1:n.61-128_61-121del