Canonical Allele Identifier: CA2338552216

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678134G= , CM000681.2:g.45678134G=	GRCh38
NC_000019.9:g.46181392G= , CM000681.1:g.46181392G=	GRCh37
NC_000019.8:g.50873232G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1060G= MANE Select	ENSP00000467494.1:p.Glu354=
ENST00000652180.1:c.877G=	ENSP00000498426.1:p.Glu293=
ENST00000263281.7:c.1060G=	ENSP00000263281.3:p.Glu354=
ENST00000304207.12:c.952G=	ENSP00000305321.8:p.Glu318=
ENST00000585889.1:c.*131G=	ENSP00000467342.1:n.*131G=
ENST00000590918.5:c.1060G=	ENSP00000467494.1:p.Glu354=
ENST00000591224.1:n.516G=
NM_000164.2:c.1060G=	NP_000155.1:p.Glu354=
NM_000164.3:c.1060G=	NP_000155.1:p.Glu354=
NM_001308418.1:c.952G=	NP_001295347.1:p.Glu318=
XM_011526709.1:c.1186G=	XP_011525011.1:p.Glu396=
XM_011526710.1:c.1186G=	XP_011525012.1:p.Glu396=
XM_011526711.1:c.1078G=	XP_011525013.1:p.Glu360=
XM_011526712.1:c.952G=	XP_011525014.1:p.Glu318=
XM_011526713.1:c.937G=	XP_011525015.1:p.Glu313=
XM_011526714.1:c.769G=	XP_011525016.1:p.Glu257=
XM_011526715.1:c.769G=	XP_011525017.1:p.Glu257=
XR_935791.1:n.1079G=
XM_011526709.2:c.1186G=	XP_011525011.1:p.Glu396=
XM_011526710.2:c.1186G=	XP_011525012.1:p.Glu396=
XM_011526711.2:c.1078G=	XP_011525013.1:p.Glu360=
XM_011526713.2:c.937G=	XP_011525015.1:p.Glu313=
XM_011526714.2:c.769G=	XP_011525016.1:p.Glu257=
XM_011526715.2:c.769G=	XP_011525017.1:p.Glu257=
XM_017026584.1:c.715G=	XP_016882073.1:p.Glu239=
XM_017026585.1:c.694G=	XP_016882074.1:p.Glu232=
XM_017026586.1:c.571G=	XP_016882075.1:p.Glu191=
XM_017026587.1:c.568G=	XP_016882076.1:p.Glu190=
XR_001753655.1:n.1155G=
XR_935791.2:n.1085G=
NM_000164.4:c.1060G= MANE Select	NP_000155.1:p.Glu354=
NM_001308418.2:c.952G=	NP_001295347.1:p.Glu318=