Canonical Allele Identifier: CA2278680001
Gene: GCGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81809840G= , CM000679.2:g.81809840G= GRCh38
NC_000017.10:g.79767716G= , CM000679.1:g.79767716G= GRCh37
NG_016409.1:g.8667G=

Transcript Alleles

HGVS Amino-acid change
ENST00000400723.8:c.119G= MANE Select ENSP00000383558.3:p.Gly40=
ENST00000400723.7:c.119G= ENSP00000383558.3:p.Gly40=
ENST00000570996.5:c.119G= ENSP00000460976.1:p.Gly40=
ENST00000572185.1:n.414G=
ENST00000573428.1:c.119G= ENSP00000458930.1:p.Gly40=
ENST00000574283.2:n.53G=
NM_000160.4:c.119G= NP_000151.1:p.Gly40=
XM_006722277.1:c.119G= XP_006722340.1:p.Gly40=
XM_011523539.1:c.-108G= XP_011521841.1:n.-108G=
XM_011523540.1:c.-398G= XP_011521842.1:n.-398G=
XM_017024446.1:c.113G= XP_016879935.1:p.Gly38=
XM_017024447.1:c.-398G= XP_016879936.1:n.-398G=
NM_000160.5:c.119G= MANE Select NP_000151.1:p.Gly40=