Canonical Allele Identifier: CA2537603753

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809637_81809638insCCTA , CM000679.2:g.81809637_81809638insCCTA	GRCh38
NC_000017.10:g.79767513_79767514insCCTA , CM000679.1:g.79767513_79767514insCCTA	GRCh37
NG_016409.1:g.8464_8465insCCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-145_61-144insCCTA MANE Select	ENSP00000383558.3:n.61-145_61-144insCCTA
ENST00000400723.7:c.61-145_61-144insCCTA	ENSP00000383558.3:n.61-145_61-144insCCTA
ENST00000570996.5:c.61-145_61-144insCCTA	ENSP00000460976.1:n.61-145_61-144insCCTA
ENST00000572185.1:n.356-145_356-144insCCTA
ENST00000573428.1:c.61-145_61-144insCCTA	ENSP00000458930.1:n.61-145_61-144insCCTA
NM_000160.4:c.61-145_61-144insCCTA	NP_000151.1:n.61-145_61-144insCCTA
XM_006722277.1:c.61-145_61-144insCCTA	XP_006722340.1:n.61-145_61-144insCCTA
XM_011523539.1:c.-166-145_-166-144insCCTA	XP_011521841.1:n.-166-145_-166-144insCCTA
XM_011523540.1:c.-456-145_-456-144insCCTA	XP_011521842.1:n.-456-145_-456-144insCCTA
XM_017024446.1:c.61-151_61-150insCCTA	XP_016879935.1:n.61-151_61-150insCCTA
XM_017024447.1:c.-450-151_-450-150insCCTA	XP_016879936.1:n.-450-151_-450-150insCCTA
NM_000160.5:c.61-145_61-144insCCTA MANE Select	NP_000151.1:n.61-145_61-144insCCTA