Canonical Allele Identifier: CA2560193448

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809624_81809631del , CM000679.2:g.81809624_81809631del	GRCh38
NC_000017.10:g.79767500_79767507del , CM000679.1:g.79767500_79767507del	GRCh37
NG_016409.1:g.8451_8458del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-158_61-151del MANE Select	ENSP00000383558.3:n.61-158_61-151del
ENST00000400723.7:c.61-158_61-151del	ENSP00000383558.3:n.61-158_61-151del
ENST00000570996.5:c.61-158_61-151del	ENSP00000460976.1:n.61-158_61-151del
ENST00000572185.1:n.356-158_356-151del
ENST00000573428.1:c.61-158_61-151del	ENSP00000458930.1:n.61-158_61-151del
NM_000160.4:c.61-158_61-151del	NP_000151.1:n.61-158_61-151del
XM_006722277.1:c.61-158_61-151del	XP_006722340.1:n.61-158_61-151del
XM_011523539.1:c.-166-158_-166-151del	XP_011521841.1:n.-166-158_-166-151del
XM_011523540.1:c.-456-158_-456-151del	XP_011521842.1:n.-456-158_-456-151del
XM_017024446.1:c.61-164_61-157del	XP_016879935.1:n.61-164_61-157del
XM_017024447.1:c.-450-164_-450-157del	XP_016879936.1:n.-450-164_-450-157del
NM_000160.5:c.61-158_61-151del MANE Select	NP_000151.1:n.61-158_61-151del