Canonical Allele Identifier: CA2338552611

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678997G= , CM000681.2:g.45678997G=	GRCh38
NC_000019.9:g.46182255G= , CM000681.1:g.46182255G=	GRCh37
NC_000019.8:g.50874095G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1152+771G= MANE Select	ENSP00000467494.1:n.1152+771G=
ENST00000652180.1:c.969+771G=	ENSP00000498426.1:n.969+771G=
ENST00000263281.7:c.1152+771G=	ENSP00000263281.3:n.1152+771G=
ENST00000304207.12:c.1044+771G=	ENSP00000305321.8:n.1044+771G=
ENST00000585889.1:c.*223+771G=	ENSP00000467342.1:n.*223+771G=
ENST00000590918.5:c.1152+771G=	ENSP00000467494.1:n.1152+771G=
NM_000164.2:c.1152+771G=	NP_000155.1:n.1152+771G=
NM_000164.3:c.1152+771G=	NP_000155.1:n.1152+771G=
NM_001308418.1:c.1044+771G=	NP_001295347.1:n.1044+771G=
XM_011526709.1:c.1278+771G=	XP_011525011.1:n.1278+771G=
XM_011526710.1:c.1278+771G=	XP_011525012.1:n.1278+771G=
XM_011526711.1:c.1170+771G=	XP_011525013.1:n.1170+771G=
XM_011526712.1:c.1044+771G=	XP_011525014.1:n.1044+771G=
XM_011526713.1:c.1029+771G=	XP_011525015.1:n.1029+771G=
XM_011526714.1:c.861+771G=	XP_011525016.1:n.861+771G=
XM_011526715.1:c.861+771G=	XP_011525017.1:n.861+771G=
XR_935791.1:n.1171+771G=
XM_011526709.2:c.1278+771G=	XP_011525011.1:n.1278+771G=
XM_011526710.2:c.1278+771G=	XP_011525012.1:n.1278+771G=
XM_011526711.2:c.1170+771G=	XP_011525013.1:n.1170+771G=
XM_011526713.2:c.1029+771G=	XP_011525015.1:n.1029+771G=
XM_011526714.2:c.861+771G=	XP_011525016.1:n.861+771G=
XM_011526715.2:c.861+771G=	XP_011525017.1:n.861+771G=
XM_017026584.1:c.807+771G=	XP_016882073.1:n.807+771G=
XM_017026585.1:c.786+771G=	XP_016882074.1:n.786+771G=
XM_017026586.1:c.663+771G=	XP_016882075.1:n.663+771G=
XM_017026587.1:c.660+771G=	XP_016882076.1:n.660+771G=
XR_001753655.1:n.1247+771G=
XR_935791.2:n.1177+771G=
NM_000164.4:c.1152+771G= MANE Select	NP_000155.1:n.1152+771G=
NM_001308418.2:c.1044+771G=	NP_001295347.1:n.1044+771G=