Canonical Allele Identifier: CA2278679839

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809642_81809646delinsTCTGC , CM000679.2:g.81809642_81809646delinsTCTGC	GRCh38
NC_000017.10:g.79767518_79767522delinsTCTGC , CM000679.1:g.79767518_79767522delinsTCTGC	GRCh37
NG_016409.1:g.8469_8473delinsTCTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-140_61-136delinsTCTGC MANE Select	ENSP00000383558.3:n.61-140_61-136delinsTCTGC
ENST00000400723.7:c.61-140_61-136delinsTCTGC	ENSP00000383558.3:n.61-140_61-136delinsTCTGC
ENST00000570996.5:c.61-140_61-136delinsTCTGC	ENSP00000460976.1:n.61-140_61-136delinsTCTGC
ENST00000572185.1:n.356-140_356-136delinsTCTGC
ENST00000573428.1:c.61-140_61-136delinsTCTGC	ENSP00000458930.1:n.61-140_61-136delinsTCTGC
NM_000160.4:c.61-140_61-136delinsTCTGC	NP_000151.1:n.61-140_61-136delinsTCTGC
XM_006722277.1:c.61-140_61-136delinsTCTGC	XP_006722340.1:n.61-140_61-136delinsTCTGC
XM_011523539.1:c.-166-140_-166-136delinsTCTGC	XP_011521841.1:n.-166-140_-166-136delinsTCTGC
XM_011523540.1:c.-456-140_-456-136delinsTCTGC	XP_011521842.1:n.-456-140_-456-136delinsTCTGC
XM_017024446.1:c.61-146_61-142delinsTCTGC	XP_016879935.1:n.61-146_61-142delinsTCTGC
XM_017024447.1:c.-450-146_-450-142delinsTCTGC	XP_016879936.1:n.-450-146_-450-142delinsTCTGC
NM_000160.5:c.61-140_61-136delinsTCTGC MANE Select	NP_000151.1:n.61-140_61-136delinsTCTGC