Canonical Allele Identifier: CA2278680017

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809889_81809890delinsGC , CM000679.2:g.81809889_81809890delinsGC	GRCh38
NC_000017.10:g.79767765_79767766delinsGC , CM000679.1:g.79767765_79767766delinsGC	GRCh37
NG_016409.1:g.8716_8717delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.163+5_163+6delinsGC MANE Select	ENSP00000383558.3:n.163+5_163+6delinsGC
ENST00000400723.7:c.163+5_163+6delinsGC	ENSP00000383558.3:n.163+5_163+6delinsGC
ENST00000570996.5:c.163+5_163+6delinsGC	ENSP00000460976.1:n.163+5_163+6delinsGC
ENST00000572185.1:n.463_464delinsGC
ENST00000573428.1:c.163+5_163+6delinsGC	ENSP00000458930.1:n.163+5_163+6delinsGC
ENST00000574283.2:n.102_103delinsGC
NM_000160.4:c.163+5_163+6delinsGC	NP_000151.1:n.163+5_163+6delinsGC
XM_006722277.1:c.163+5_163+6delinsGC	XP_006722340.1:n.163+5_163+6delinsGC
XM_011523539.1:c.-59_-58delinsGC	XP_011521841.1:n.-59_-58delinsGC
XM_011523540.1:c.-349_-348delinsGC	XP_011521842.1:n.-349_-348delinsGC
XM_017024446.1:c.157+5_157+6delinsGC	XP_016879935.1:n.157+5_157+6delinsGC
XM_017024447.1:c.-349_-348delinsGC	XP_016879936.1:n.-349_-348delinsGC
NM_000160.5:c.163+5_163+6delinsGC MANE Select	NP_000151.1:n.163+5_163+6delinsGC