Canonical Allele Identifier: CA2278680002
Gene: GCGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81809844C= , CM000679.2:g.81809844C= GRCh38
NC_000017.10:g.79767720C= , CM000679.1:g.79767720C= GRCh37
NG_016409.1:g.8671C=

Transcript Alleles

HGVS Amino-acid change
ENST00000400723.8:c.123C= MANE Select ENSP00000383558.3:p.Asp41=
ENST00000400723.7:c.123C= ENSP00000383558.3:p.Asp41=
ENST00000570996.5:c.123C= ENSP00000460976.1:p.Asp41=
ENST00000572185.1:n.418C=
ENST00000573428.1:c.123C= ENSP00000458930.1:p.Asp41=
ENST00000574283.2:n.57C=
NM_000160.4:c.123C= NP_000151.1:p.Asp41=
XM_006722277.1:c.123C= XP_006722340.1:p.Asp41=
XM_011523539.1:c.-104C= XP_011521841.1:n.-104C=
XM_011523540.1:c.-394C= XP_011521842.1:n.-394C=
XM_017024446.1:c.117C= XP_016879935.1:p.Asp39=
XM_017024447.1:c.-394C= XP_016879936.1:n.-394C=
NM_000160.5:c.123C= MANE Select NP_000151.1:p.Asp41=