Canonical Allele Identifier: CA2278679808

Gene: GCGR

Linked Data

• dbSNP Id: rs2038048780

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809620_81809623del , CM000679.2:g.81809620_81809623del	GRCh38
NC_000017.10:g.79767496_79767499del , CM000679.1:g.79767496_79767499del	GRCh37
NG_016409.1:g.8447_8450del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-162_61-159del MANE Select	ENSP00000383558.3:n.61-162_61-159del
ENST00000400723.7:c.61-162_61-159del	ENSP00000383558.3:n.61-162_61-159del
ENST00000570996.5:c.61-162_61-159del	ENSP00000460976.1:n.61-162_61-159del
ENST00000572185.1:n.356-162_356-159del
ENST00000573428.1:c.61-162_61-159del	ENSP00000458930.1:n.61-162_61-159del
NM_000160.4:c.61-162_61-159del	NP_000151.1:n.61-162_61-159del
XM_006722277.1:c.61-162_61-159del	XP_006722340.1:n.61-162_61-159del
XM_011523539.1:c.-166-162_-166-159del	XP_011521841.1:n.-166-162_-166-159del
XM_011523540.1:c.-456-162_-456-159del	XP_011521842.1:n.-456-162_-456-159del
XM_017024446.1:c.61-168_61-165del	XP_016879935.1:n.61-168_61-165del
XM_017024447.1:c.-450-168_-450-165del	XP_016879936.1:n.-450-168_-450-165del
NM_000160.5:c.61-162_61-159del MANE Select	NP_000151.1:n.61-162_61-159del