Canonical Allele Identifier: CA2338552224

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678151C= , CM000681.2:g.45678151C=	GRCh38
NC_000019.9:g.46181409C= , CM000681.1:g.46181409C=	GRCh37
NC_000019.8:g.50873249C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1077C= MANE Select	ENSP00000467494.1:p.Pro359=
ENST00000652180.1:c.894C=	ENSP00000498426.1:p.Pro298=
ENST00000263281.7:c.1077C=	ENSP00000263281.3:p.Pro359=
ENST00000304207.12:c.969C=	ENSP00000305321.8:p.Pro323=
ENST00000585889.1:c.*148C=	ENSP00000467342.1:n.*148C=
ENST00000590918.5:c.1077C=	ENSP00000467494.1:p.Pro359=
ENST00000591224.1:n.533C=
NM_000164.2:c.1077C=	NP_000155.1:p.Pro359=
NM_000164.3:c.1077C=	NP_000155.1:p.Pro359=
NM_001308418.1:c.969C=	NP_001295347.1:p.Pro323=
XM_011526709.1:c.1203C=	XP_011525011.1:p.Pro401=
XM_011526710.1:c.1203C=	XP_011525012.1:p.Pro401=
XM_011526711.1:c.1095C=	XP_011525013.1:p.Pro365=
XM_011526712.1:c.969C=	XP_011525014.1:p.Pro323=
XM_011526713.1:c.954C=	XP_011525015.1:p.Pro318=
XM_011526714.1:c.786C=	XP_011525016.1:p.Pro262=
XM_011526715.1:c.786C=	XP_011525017.1:p.Pro262=
XR_935791.1:n.1096C=
XM_011526709.2:c.1203C=	XP_011525011.1:p.Pro401=
XM_011526710.2:c.1203C=	XP_011525012.1:p.Pro401=
XM_011526711.2:c.1095C=	XP_011525013.1:p.Pro365=
XM_011526713.2:c.954C=	XP_011525015.1:p.Pro318=
XM_011526714.2:c.786C=	XP_011525016.1:p.Pro262=
XM_011526715.2:c.786C=	XP_011525017.1:p.Pro262=
XM_017026584.1:c.732C=	XP_016882073.1:p.Pro244=
XM_017026585.1:c.711C=	XP_016882074.1:p.Pro237=
XM_017026586.1:c.588C=	XP_016882075.1:p.Pro196=
XM_017026587.1:c.585C=	XP_016882076.1:p.Pro195=
XR_001753655.1:n.1172C=
XR_935791.2:n.1102C=
NM_000164.4:c.1077C= MANE Select	NP_000155.1:p.Pro359=
NM_001308418.2:c.969C=	NP_001295347.1:p.Pro323=