Canonical Allele Identifier: CA2338552141

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677978_45677979delinsCG , CM000681.2:g.45677978_45677979delinsCG	GRCh38
NC_000019.9:g.46181236_46181237delinsCG , CM000681.1:g.46181236_46181237delinsCG	GRCh37
NC_000019.8:g.50873076_50873077delinsCG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.997_998delinsCG MANE Select	ENSP00000467494.1:p.Arg333=
ENST00000652180.1:c.814_815delinsCG	ENSP00000498426.1:p.Arg272=
ENST00000263281.7:c.997_998delinsCG	ENSP00000263281.3:p.Arg333=
ENST00000304207.12:c.889_890delinsCG	ENSP00000305321.8:p.Arg297=
ENST00000585889.1:c.*68_*69delinsCG	ENSP00000467342.1:n.*68_*69delinsCG
ENST00000590918.5:c.997_998delinsCG	ENSP00000467494.1:p.Arg333=
ENST00000591224.1:n.453_454delinsCG
ENST00000593127.1:n.98_99delinsCG
NM_000164.2:c.997_998delinsCG	NP_000155.1:p.Arg333=
NM_000164.3:c.997_998delinsCG	NP_000155.1:p.Arg333=
NM_001308418.1:c.889_890delinsCG	NP_001295347.1:p.Arg297=
XM_011526709.1:c.1123_1124delinsCG	XP_011525011.1:p.Arg375=
XM_011526710.1:c.1123_1124delinsCG	XP_011525012.1:p.Arg375=
XM_011526711.1:c.1015_1016delinsCG	XP_011525013.1:p.Arg339=
XM_011526712.1:c.889_890delinsCG	XP_011525014.1:p.Arg297=
XM_011526713.1:c.874_875delinsCG	XP_011525015.1:p.Arg292=
XM_011526714.1:c.706_707delinsCG	XP_011525016.1:p.Arg236=
XM_011526715.1:c.706_707delinsCG	XP_011525017.1:p.Arg236=
XM_011526716.1:c.*81_*82delinsCG	XP_011525018.1:n.*81_*82delinsCG
XM_011526717.1:c.*81_*82delinsCG	XP_011525019.1:n.*81_*82delinsCG
XR_935791.1:n.1016_1017delinsCG
XM_011526709.2:c.1123_1124delinsCG	XP_011525011.1:p.Arg375=
XM_011526710.2:c.1123_1124delinsCG	XP_011525012.1:p.Arg375=
XM_011526711.2:c.1015_1016delinsCG	XP_011525013.1:p.Arg339=
XM_011526713.2:c.874_875delinsCG	XP_011525015.1:p.Arg292=
XM_011526714.2:c.706_707delinsCG	XP_011525016.1:p.Arg236=
XM_011526715.2:c.706_707delinsCG	XP_011525017.1:p.Arg236=
XM_011526716.2:c.*81_*82delinsCG	XP_011525018.1:n.*81_*82delinsCG
XM_017026584.1:c.652_653delinsCG	XP_016882073.1:p.Arg218=
XM_017026585.1:c.631_632delinsCG	XP_016882074.1:p.Arg211=
XM_017026586.1:c.508_509delinsCG	XP_016882075.1:p.Arg170=
XM_017026587.1:c.505_506delinsCG	XP_016882076.1:p.Arg169=
XR_001753655.1:n.1092_1093delinsCG
XR_935791.2:n.1022_1023delinsCG
NM_000164.4:c.997_998delinsCG MANE Select	NP_000155.1:p.Arg333=
NM_001308418.2:c.889_890delinsCG	NP_001295347.1:p.Arg297=