Canonical Allele Identifier: CA2338552126

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677953G= , CM000681.2:g.45677953G=	GRCh38
NC_000019.9:g.46181211G= , CM000681.1:g.46181211G=	GRCh37
NC_000019.8:g.50873051G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.972G= MANE Select	ENSP00000467494.1:p.Lys324=
ENST00000652180.1:c.789G=	ENSP00000498426.1:p.Lys263=
ENST00000263281.7:c.972G=	ENSP00000263281.3:p.Lys324=
ENST00000304207.12:c.864G=	ENSP00000305321.8:p.Lys288=
ENST00000585889.1:c.*43G=	ENSP00000467342.1:n.*43G=
ENST00000590918.5:c.972G=	ENSP00000467494.1:p.Lys324=
ENST00000591224.1:n.428G=
ENST00000593127.1:n.73G=
NM_000164.2:c.972G=	NP_000155.1:p.Lys324=
NM_000164.3:c.972G=	NP_000155.1:p.Lys324=
NM_001308418.1:c.864G=	NP_001295347.1:p.Lys288=
XM_011526709.1:c.1098G=	XP_011525011.1:p.Lys366=
XM_011526710.1:c.1098G=	XP_011525012.1:p.Lys366=
XM_011526711.1:c.990G=	XP_011525013.1:p.Lys330=
XM_011526712.1:c.864G=	XP_011525014.1:p.Lys288=
XM_011526713.1:c.849G=	XP_011525015.1:p.Lys283=
XM_011526714.1:c.681G=	XP_011525016.1:p.Lys227=
XM_011526715.1:c.681G=	XP_011525017.1:p.Lys227=
XM_011526716.1:c.*56G=	XP_011525018.1:n.*56G=
XM_011526717.1:c.*56G=	XP_011525019.1:n.*56G=
XR_935791.1:n.991G=
XM_011526709.2:c.1098G=	XP_011525011.1:p.Lys366=
XM_011526710.2:c.1098G=	XP_011525012.1:p.Lys366=
XM_011526711.2:c.990G=	XP_011525013.1:p.Lys330=
XM_011526713.2:c.849G=	XP_011525015.1:p.Lys283=
XM_011526714.2:c.681G=	XP_011525016.1:p.Lys227=
XM_011526715.2:c.681G=	XP_011525017.1:p.Lys227=
XM_011526716.2:c.*56G=	XP_011525018.1:n.*56G=
XM_017026584.1:c.627G=	XP_016882073.1:p.Lys209=
XM_017026585.1:c.606G=	XP_016882074.1:p.Lys202=
XM_017026586.1:c.483G=	XP_016882075.1:p.Lys161=
XM_017026587.1:c.480G=	XP_016882076.1:p.Lys160=
XR_001753655.1:n.1067G=
XR_935791.2:n.997G=
NM_000164.4:c.972G= MANE Select	NP_000155.1:p.Lys324=
NM_001308418.2:c.864G=	NP_001295347.1:p.Lys288=