Canonical Allele Identifier: CA2338552142

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677978C= , CM000681.2:g.45677978C=	GRCh38
NC_000019.9:g.46181236C= , CM000681.1:g.46181236C=	GRCh37
NC_000019.8:g.50873076C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.997C= MANE Select	ENSP00000467494.1:p.Arg333=
ENST00000652180.1:c.814C=	ENSP00000498426.1:p.Arg272=
ENST00000263281.7:c.997C=	ENSP00000263281.3:p.Arg333=
ENST00000304207.12:c.889C=	ENSP00000305321.8:p.Arg297=
ENST00000585889.1:c.*68C=	ENSP00000467342.1:n.*68C=
ENST00000590918.5:c.997C=	ENSP00000467494.1:p.Arg333=
ENST00000591224.1:n.453C=
ENST00000593127.1:n.98C=
NM_000164.2:c.997C=	NP_000155.1:p.Arg333=
NM_000164.3:c.997C=	NP_000155.1:p.Arg333=
NM_001308418.1:c.889C=	NP_001295347.1:p.Arg297=
XM_011526709.1:c.1123C=	XP_011525011.1:p.Arg375=
XM_011526710.1:c.1123C=	XP_011525012.1:p.Arg375=
XM_011526711.1:c.1015C=	XP_011525013.1:p.Arg339=
XM_011526712.1:c.889C=	XP_011525014.1:p.Arg297=
XM_011526713.1:c.874C=	XP_011525015.1:p.Arg292=
XM_011526714.1:c.706C=	XP_011525016.1:p.Arg236=
XM_011526715.1:c.706C=	XP_011525017.1:p.Arg236=
XM_011526716.1:c.*81C=	XP_011525018.1:n.*81C=
XM_011526717.1:c.*81C=	XP_011525019.1:n.*81C=
XR_935791.1:n.1016C=
XM_011526709.2:c.1123C=	XP_011525011.1:p.Arg375=
XM_011526710.2:c.1123C=	XP_011525012.1:p.Arg375=
XM_011526711.2:c.1015C=	XP_011525013.1:p.Arg339=
XM_011526713.2:c.874C=	XP_011525015.1:p.Arg292=
XM_011526714.2:c.706C=	XP_011525016.1:p.Arg236=
XM_011526715.2:c.706C=	XP_011525017.1:p.Arg236=
XM_011526716.2:c.*81C=	XP_011525018.1:n.*81C=
XM_017026584.1:c.652C=	XP_016882073.1:p.Arg218=
XM_017026585.1:c.631C=	XP_016882074.1:p.Arg211=
XM_017026586.1:c.508C=	XP_016882075.1:p.Arg170=
XM_017026587.1:c.505C=	XP_016882076.1:p.Arg169=
XR_001753655.1:n.1092C=
XR_935791.2:n.1022C=
NM_000164.4:c.997C= MANE Select	NP_000155.1:p.Arg333=
NM_001308418.2:c.889C=	NP_001295347.1:p.Arg297=