Canonical Allele Identifier: CA2338552128

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677955T= , CM000681.2:g.45677955T=	GRCh38
NC_000019.9:g.46181213T= , CM000681.1:g.46181213T=	GRCh37
NC_000019.8:g.50873053T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.974T= MANE Select	ENSP00000467494.1:p.Leu325=
ENST00000652180.1:c.791T=	ENSP00000498426.1:p.Leu264=
ENST00000263281.7:c.974T=	ENSP00000263281.3:p.Leu325=
ENST00000304207.12:c.866T=	ENSP00000305321.8:p.Leu289=
ENST00000585889.1:c.*45T=	ENSP00000467342.1:n.*45T=
ENST00000590918.5:c.974T=	ENSP00000467494.1:p.Leu325=
ENST00000591224.1:n.430T=
ENST00000593127.1:n.75T=
NM_000164.2:c.974T=	NP_000155.1:p.Leu325=
NM_000164.3:c.974T=	NP_000155.1:p.Leu325=
NM_001308418.1:c.866T=	NP_001295347.1:p.Leu289=
XM_011526709.1:c.1100T=	XP_011525011.1:p.Leu367=
XM_011526710.1:c.1100T=	XP_011525012.1:p.Leu367=
XM_011526711.1:c.992T=	XP_011525013.1:p.Leu331=
XM_011526712.1:c.866T=	XP_011525014.1:p.Leu289=
XM_011526713.1:c.851T=	XP_011525015.1:p.Leu284=
XM_011526714.1:c.683T=	XP_011525016.1:p.Leu228=
XM_011526715.1:c.683T=	XP_011525017.1:p.Leu228=
XM_011526716.1:c.*58T=	XP_011525018.1:n.*58T=
XM_011526717.1:c.*58T=	XP_011525019.1:n.*58T=
XR_935791.1:n.993T=
XM_011526709.2:c.1100T=	XP_011525011.1:p.Leu367=
XM_011526710.2:c.1100T=	XP_011525012.1:p.Leu367=
XM_011526711.2:c.992T=	XP_011525013.1:p.Leu331=
XM_011526713.2:c.851T=	XP_011525015.1:p.Leu284=
XM_011526714.2:c.683T=	XP_011525016.1:p.Leu228=
XM_011526715.2:c.683T=	XP_011525017.1:p.Leu228=
XM_011526716.2:c.*58T=	XP_011525018.1:n.*58T=
XM_017026584.1:c.629T=	XP_016882073.1:p.Leu210=
XM_017026585.1:c.608T=	XP_016882074.1:p.Leu203=
XM_017026586.1:c.485T=	XP_016882075.1:p.Leu162=
XM_017026587.1:c.482T=	XP_016882076.1:p.Leu161=
XR_001753655.1:n.1069T=
XR_935791.2:n.999T=
NM_000164.4:c.974T= MANE Select	NP_000155.1:p.Leu325=
NM_001308418.2:c.866T=	NP_001295347.1:p.Leu289=