Canonical Allele Identifier: CA2338552220

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678140G= , CM000681.2:g.45678140G=	GRCh38
NC_000019.9:g.46181398G= , CM000681.1:g.46181398G=	GRCh37
NC_000019.8:g.50873238G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1066G= MANE Select	ENSP00000467494.1:p.Val356=
ENST00000652180.1:c.883G=	ENSP00000498426.1:p.Val295=
ENST00000263281.7:c.1066G=	ENSP00000263281.3:p.Val356=
ENST00000304207.12:c.958G=	ENSP00000305321.8:p.Val320=
ENST00000585889.1:c.*137G=	ENSP00000467342.1:n.*137G=
ENST00000590918.5:c.1066G=	ENSP00000467494.1:p.Val356=
ENST00000591224.1:n.522G=
NM_000164.2:c.1066G=	NP_000155.1:p.Val356=
NM_000164.3:c.1066G=	NP_000155.1:p.Val356=
NM_001308418.1:c.958G=	NP_001295347.1:p.Val320=
XM_011526709.1:c.1192G=	XP_011525011.1:p.Val398=
XM_011526710.1:c.1192G=	XP_011525012.1:p.Val398=
XM_011526711.1:c.1084G=	XP_011525013.1:p.Val362=
XM_011526712.1:c.958G=	XP_011525014.1:p.Val320=
XM_011526713.1:c.943G=	XP_011525015.1:p.Val315=
XM_011526714.1:c.775G=	XP_011525016.1:p.Val259=
XM_011526715.1:c.775G=	XP_011525017.1:p.Val259=
XR_935791.1:n.1085G=
XM_011526709.2:c.1192G=	XP_011525011.1:p.Val398=
XM_011526710.2:c.1192G=	XP_011525012.1:p.Val398=
XM_011526711.2:c.1084G=	XP_011525013.1:p.Val362=
XM_011526713.2:c.943G=	XP_011525015.1:p.Val315=
XM_011526714.2:c.775G=	XP_011525016.1:p.Val259=
XM_011526715.2:c.775G=	XP_011525017.1:p.Val259=
XM_017026584.1:c.721G=	XP_016882073.1:p.Val241=
XM_017026585.1:c.700G=	XP_016882074.1:p.Val234=
XM_017026586.1:c.577G=	XP_016882075.1:p.Val193=
XM_017026587.1:c.574G=	XP_016882076.1:p.Val192=
XR_001753655.1:n.1161G=
XR_935791.2:n.1091G=
NM_000164.4:c.1066G= MANE Select	NP_000155.1:p.Val356=
NM_001308418.2:c.958G=	NP_001295347.1:p.Val320=