Canonical Allele Identifier: CA8841983
Gene: GCGR HGNC NCBI

Linked Data

dbSNP Id: rs762597738
ExAC: 17:79767614 C / CCTGT
gnomAD v2: 17-79767614-C-CCTGT
gnomAD v3: 17-81809738-C-CCTGT
gnomAD v4: 17-81809738-C-CCTGT
MyVariant Identifiers: chr17:g.79767622_79767623insCTGT (hg19) chr17:g.79767618_79767619insCTGT (hg19) chr17:g.79767614_79767615insCTGT (hg19) chr17:g.81809742_81809743insCTGT (hg38) chr17:g.81809738_81809739insCTGT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81809754_81809757dup , CM000679.2:g.81809754_81809757dup GRCh38
NC_000017.10:g.79767630_79767633dup , CM000679.1:g.79767630_79767633dup GRCh37
NG_016409.1:g.8581_8584dup

Transcript Alleles

HGVS Amino-acid change
ENST00000400723.8:c.61-28_61-25dup MANE Select ENSP00000383558.3:n.61-28_61-25dup
ENST00000400723.7:c.61-28_61-25dup ENSP00000383558.3:n.61-28_61-25dup
ENST00000570996.5:c.61-28_61-25dup ENSP00000460976.1:n.61-28_61-25dup
ENST00000572185.1:n.356-28_356-25dup
ENST00000573428.1:c.61-28_61-25dup ENSP00000458930.1:n.61-28_61-25dup
NM_000160.4:c.61-28_61-25dup NP_000151.1:n.61-28_61-25dup
XM_006722277.1:c.61-28_61-25dup XP_006722340.1:n.61-28_61-25dup
XM_011523539.1:c.-166-28_-166-25dup XP_011521841.1:n.-166-28_-166-25dup
XM_011523540.1:c.-456-28_-456-25dup XP_011521842.1:n.-456-28_-456-25dup
XM_017024446.1:c.61-34_61-31dup XP_016879935.1:n.61-34_61-31dup
XM_017024447.1:c.-450-34_-450-31dup XP_016879936.1:n.-450-34_-450-31dup
NM_000160.5:c.61-28_61-25dup MANE Select NP_000151.1:n.61-28_61-25dup
Search 100 bp 5'
Search 100 bp 3'