Canonical Allele Identifier: CA8842063

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81811302C>T , CM000679.2:g.81811302C>T	GRCh38
NC_000017.10:g.79769178C>T , CM000679.1:g.79769178C>T	GRCh37
NG_016409.1:g.10129C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000160.5:c.474C>T MANE Select	NP_000151.1:p.Leu158=
ENST00000400723.8:c.474C>T MANE Select	ENSP00000383558.3:p.Leu158=
NM_000160.4:c.474C>T	NP_000151.1:p.Leu158=
ENST00000400723.7:c.474C>T	ENSP00000383558.3:p.Leu158=
ENST00000570996.5:c.474C>T	ENSP00000460976.1:p.Leu158=
ENST00000574283.2:n.648C>T
XM_006722277.1:c.474C>T	XP_006722340.1:p.Leu158=
XM_011523539.1:c.375C>T	XP_011521841.1:p.Leu125=
XM_011523540.1:c.108C>T	XP_011521842.1:p.Leu36=
XM_017024446.1:c.468C>T	XP_016879935.1:p.Leu156=
XM_017024447.1:c.108C>T	XP_016879936.1:p.Leu36=