Canonical Allele Identifier: CA627768187

Gene: GCGR

Linked Data

• dbSNP Id: rs1451153335
• gnomAD v2: 17-79767494-TCTGTCCGTCTGCCTGC-T
• MyVariant Identifiers: chr17:g.79767495_79767510del (hg19) ; chr17:g.81809619_81809634del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809624_81809639del , CM000679.2:g.81809624_81809639del	GRCh38
NC_000017.10:g.79767500_79767515del , CM000679.1:g.79767500_79767515del	GRCh37
NG_016409.1:g.8451_8466del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-158_61-143del MANE Select	ENSP00000383558.3:n.61-158_61-143del
ENST00000400723.7:c.61-158_61-143del	ENSP00000383558.3:n.61-158_61-143del
ENST00000570996.5:c.61-158_61-143del	ENSP00000460976.1:n.61-158_61-143del
ENST00000572185.1:n.356-158_356-143del
ENST00000573428.1:c.61-158_61-143del	ENSP00000458930.1:n.61-158_61-143del
NM_000160.4:c.61-158_61-143del	NP_000151.1:n.61-158_61-143del
XM_006722277.1:c.61-158_61-143del	XP_006722340.1:n.61-158_61-143del
XM_011523539.1:c.-166-158_-166-143del	XP_011521841.1:n.-166-158_-166-143del
XM_011523540.1:c.-456-158_-456-143del	XP_011521842.1:n.-456-158_-456-143del
XM_017024446.1:c.61-164_61-149del	XP_016879935.1:n.61-164_61-149del
XM_017024447.1:c.-450-164_-450-149del	XP_016879936.1:n.-450-164_-450-149del
NM_000160.5:c.61-158_61-143del MANE Select	NP_000151.1:n.61-158_61-143del