Canonical Allele Identifier: CA2338552130

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677959G= , CM000681.2:g.45677959G=	GRCh38
NC_000019.9:g.46181217G= , CM000681.1:g.46181217G=	GRCh37
NC_000019.8:g.50873057G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.978G= MANE Select	ENSP00000467494.1:p.Arg326=
ENST00000652180.1:c.795G=	ENSP00000498426.1:p.Arg265=
ENST00000263281.7:c.978G=	ENSP00000263281.3:p.Arg326=
ENST00000304207.12:c.870G=	ENSP00000305321.8:p.Arg290=
ENST00000585889.1:c.*49G=	ENSP00000467342.1:n.*49G=
ENST00000590918.5:c.978G=	ENSP00000467494.1:p.Arg326=
ENST00000591224.1:n.434G=
ENST00000593127.1:n.79G=
NM_000164.2:c.978G=	NP_000155.1:p.Arg326=
NM_000164.3:c.978G=	NP_000155.1:p.Arg326=
NM_001308418.1:c.870G=	NP_001295347.1:p.Arg290=
XM_011526709.1:c.1104G=	XP_011525011.1:p.Arg368=
XM_011526710.1:c.1104G=	XP_011525012.1:p.Arg368=
XM_011526711.1:c.996G=	XP_011525013.1:p.Arg332=
XM_011526712.1:c.870G=	XP_011525014.1:p.Arg290=
XM_011526713.1:c.855G=	XP_011525015.1:p.Arg285=
XM_011526714.1:c.687G=	XP_011525016.1:p.Arg229=
XM_011526715.1:c.687G=	XP_011525017.1:p.Arg229=
XM_011526716.1:c.*62G=	XP_011525018.1:n.*62G=
XM_011526717.1:c.*62G=	XP_011525019.1:n.*62G=
XR_935791.1:n.997G=
XM_011526709.2:c.1104G=	XP_011525011.1:p.Arg368=
XM_011526710.2:c.1104G=	XP_011525012.1:p.Arg368=
XM_011526711.2:c.996G=	XP_011525013.1:p.Arg332=
XM_011526713.2:c.855G=	XP_011525015.1:p.Arg285=
XM_011526714.2:c.687G=	XP_011525016.1:p.Arg229=
XM_011526715.2:c.687G=	XP_011525017.1:p.Arg229=
XM_011526716.2:c.*62G=	XP_011525018.1:n.*62G=
XM_017026584.1:c.633G=	XP_016882073.1:p.Arg211=
XM_017026585.1:c.612G=	XP_016882074.1:p.Arg204=
XM_017026586.1:c.489G=	XP_016882075.1:p.Arg163=
XM_017026587.1:c.486G=	XP_016882076.1:p.Arg162=
XR_001753655.1:n.1073G=
XR_935791.2:n.1003G=
NM_000164.4:c.978G= MANE Select	NP_000155.1:p.Arg326=
NM_001308418.2:c.870G=	NP_001295347.1:p.Arg290=