Canonical Allele Identifier: CA2278679928

Gene: GCGR

Linked Data

• dbSNP Id: rs2038054169
• gnomAD v4: 17-81809730-T-TCTGC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809738_81809741dup , CM000679.2:g.81809738_81809741dup	GRCh38
NC_000017.10:g.79767614_79767617dup , CM000679.1:g.79767614_79767617dup	GRCh37
NG_016409.1:g.8565_8568dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000400723.8:c.61-44_61-41dup MANE Select	ENSP00000383558.3:n.61-44_61-41dup
ENST00000400723.7:c.61-44_61-41dup	ENSP00000383558.3:n.61-44_61-41dup
ENST00000570996.5:c.61-44_61-41dup	ENSP00000460976.1:n.61-44_61-41dup
ENST00000572185.1:n.356-44_356-41dup
ENST00000573428.1:c.61-44_61-41dup	ENSP00000458930.1:n.61-44_61-41dup
NM_000160.4:c.61-44_61-41dup	NP_000151.1:n.61-44_61-41dup
XM_006722277.1:c.61-44_61-41dup	XP_006722340.1:n.61-44_61-41dup
XM_011523539.1:c.-166-44_-166-41dup	XP_011521841.1:n.-166-44_-166-41dup
XM_011523540.1:c.-456-44_-456-41dup	XP_011521842.1:n.-456-44_-456-41dup
XM_017024446.1:c.61-50_61-47dup	XP_016879935.1:n.61-50_61-47dup
XM_017024447.1:c.-450-50_-450-47dup	XP_016879936.1:n.-450-50_-450-47dup
NM_000160.5:c.61-44_61-41dup MANE Select	NP_000151.1:n.61-44_61-41dup