Canonical Allele Identifier: CA2278679831
Gene: GCGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81809634_81809642delinsCCTGTCTGT , CM000679.2:g.81809634_81809642delinsCCTGTCTGT GRCh38
NC_000017.10:g.79767510_79767518delinsCCTGTCTGT , CM000679.1:g.79767510_79767518delinsCCTGTCTGT GRCh37
NG_016409.1:g.8461_8469delinsCCTGTCTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000400723.8:c.61-148_61-140delinsCCTGTCTGT MANE Select ENSP00000383558.3:n.61-148_61-140delinsCCTGTCTGT
ENST00000400723.7:c.61-148_61-140delinsCCTGTCTGT ENSP00000383558.3:n.61-148_61-140delinsCCTGTCTGT
ENST00000570996.5:c.61-148_61-140delinsCCTGTCTGT ENSP00000460976.1:n.61-148_61-140delinsCCTGTCTGT
ENST00000572185.1:n.356-148_356-140delinsCCTGTCTGT
ENST00000573428.1:c.61-148_61-140delinsCCTGTCTGT ENSP00000458930.1:n.61-148_61-140delinsCCTGTCTGT
NM_000160.4:c.61-148_61-140delinsCCTGTCTGT NP_000151.1:n.61-148_61-140delinsCCTGTCTGT
XM_006722277.1:c.61-148_61-140delinsCCTGTCTGT XP_006722340.1:n.61-148_61-140delinsCCTGTCTGT
XM_011523539.1:c.-166-148_-166-140delinsCCTGTCTGT XP_011521841.1:n.-166-148_-166-140delinsCCTGTCTGT
XM_011523540.1:c.-456-148_-456-140delinsCCTGTCTGT XP_011521842.1:n.-456-148_-456-140delinsCCTGTCTGT
XM_017024446.1:c.61-154_61-146delinsCCTGTCTGT XP_016879935.1:n.61-154_61-146delinsCCTGTCTGT
XM_017024447.1:c.-450-154_-450-146delinsCCTGTCTGT XP_016879936.1:n.-450-154_-450-146delinsCCTGTCTGT
NM_000160.5:c.61-148_61-140delinsCCTGTCTGT MANE Select NP_000151.1:n.61-148_61-140delinsCCTGTCTGT