Canonical Allele Identifier: CA775687637

Gene: GCGR

Linked Data

• dbSNP Id: rs1401432807
• gnomAD v4: 17-81809658-TCTGTCTGC-T
• MyVariant Identifiers: chr17:g.79767535_79767542del (hg19) ; chr17:g.81809659_81809666del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809666_81809673del , CM000679.2:g.81809666_81809673del	GRCh38
NC_000017.10:g.79767542_79767549del , CM000679.1:g.79767542_79767549del	GRCh37
NG_016409.1:g.8493_8500del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-116_61-109del MANE Select	ENSP00000383558.3:n.61-116_61-109del
ENST00000400723.7:c.61-116_61-109del	ENSP00000383558.3:n.61-116_61-109del
ENST00000570996.5:c.61-116_61-109del	ENSP00000460976.1:n.61-116_61-109del
ENST00000572185.1:n.356-116_356-109del
ENST00000573428.1:c.61-116_61-109del	ENSP00000458930.1:n.61-116_61-109del
NM_000160.4:c.61-116_61-109del	NP_000151.1:n.61-116_61-109del
XM_006722277.1:c.61-116_61-109del	XP_006722340.1:n.61-116_61-109del
XM_011523539.1:c.-166-116_-166-109del	XP_011521841.1:n.-166-116_-166-109del
XM_011523540.1:c.-456-116_-456-109del	XP_011521842.1:n.-456-116_-456-109del
XM_017024446.1:c.61-122_61-115del	XP_016879935.1:n.61-122_61-115del
XM_017024447.1:c.-450-122_-450-115del	XP_016879936.1:n.-450-122_-450-115del
NM_000160.5:c.61-116_61-109del MANE Select	NP_000151.1:n.61-116_61-109del