Canonical Allele Identifier: CA2500496932

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809574_81809633dup , CM000679.2:g.81809574_81809633dup	GRCh38
NC_000017.10:g.79767450_79767509dup , CM000679.1:g.79767450_79767509dup	GRCh37
NG_016409.1:g.8401_8460dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-208_61-149dup MANE Select	ENSP00000383558.3:n.61-208_61-149dup
ENST00000400723.7:c.61-208_61-149dup	ENSP00000383558.3:n.61-208_61-149dup
ENST00000570996.5:c.61-208_61-149dup	ENSP00000460976.1:n.61-208_61-149dup
ENST00000572185.1:n.356-208_356-149dup
ENST00000573428.1:c.61-208_61-149dup	ENSP00000458930.1:n.61-208_61-149dup
NM_000160.4:c.61-208_61-149dup	NP_000151.1:n.61-208_61-149dup
XM_006722277.1:c.61-208_61-149dup	XP_006722340.1:n.61-208_61-149dup
XM_011523539.1:c.-166-208_-166-149dup	XP_011521841.1:n.-166-208_-166-149dup
XM_011523540.1:c.-456-208_-456-149dup	XP_011521842.1:n.-456-208_-456-149dup
XM_017024446.1:c.61-214_61-155dup	XP_016879935.1:n.61-214_61-155dup
XM_017024447.1:c.-450-214_-450-155dup	XP_016879936.1:n.-450-214_-450-155dup
NM_000160.5:c.61-208_61-149dup MANE Select	NP_000151.1:n.61-208_61-149dup