Canonical Allele Identifier: CA2338552144

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677982A= , CM000681.2:g.45677982A=	GRCh38
NC_000019.9:g.46181240A= , CM000681.1:g.46181240A=	GRCh37
NC_000019.8:g.50873080A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1001A= MANE Select	ENSP00000467494.1:p.Asp334=
ENST00000652180.1:c.818A=	ENSP00000498426.1:p.Asp273=
ENST00000263281.7:c.1001A=	ENSP00000263281.3:p.Asp334=
ENST00000304207.12:c.893A=	ENSP00000305321.8:p.Asp298=
ENST00000585889.1:c.*72A=	ENSP00000467342.1:n.*72A=
ENST00000590918.5:c.1001A=	ENSP00000467494.1:p.Asp334=
ENST00000591224.1:n.457A=
ENST00000593127.1:n.102A=
NM_000164.2:c.1001A=	NP_000155.1:p.Asp334=
NM_000164.3:c.1001A=	NP_000155.1:p.Asp334=
NM_001308418.1:c.893A=	NP_001295347.1:p.Asp298=
XM_011526709.1:c.1127A=	XP_011525011.1:p.Asp376=
XM_011526710.1:c.1127A=	XP_011525012.1:p.Asp376=
XM_011526711.1:c.1019A=	XP_011525013.1:p.Asp340=
XM_011526712.1:c.893A=	XP_011525014.1:p.Asp298=
XM_011526713.1:c.878A=	XP_011525015.1:p.Asp293=
XM_011526714.1:c.710A=	XP_011525016.1:p.Asp237=
XM_011526715.1:c.710A=	XP_011525017.1:p.Asp237=
XM_011526716.1:c.*85A=	XP_011525018.1:n.*85A=
XM_011526717.1:c.*85A=	XP_011525019.1:n.*85A=
XR_935791.1:n.1020A=
XM_011526709.2:c.1127A=	XP_011525011.1:p.Asp376=
XM_011526710.2:c.1127A=	XP_011525012.1:p.Asp376=
XM_011526711.2:c.1019A=	XP_011525013.1:p.Asp340=
XM_011526713.2:c.878A=	XP_011525015.1:p.Asp293=
XM_011526714.2:c.710A=	XP_011525016.1:p.Asp237=
XM_011526715.2:c.710A=	XP_011525017.1:p.Asp237=
XM_011526716.2:c.*85A=	XP_011525018.1:n.*85A=
XM_017026584.1:c.656A=	XP_016882073.1:p.Asp219=
XM_017026585.1:c.635A=	XP_016882074.1:p.Asp212=
XM_017026586.1:c.512A=	XP_016882075.1:p.Asp171=
XM_017026587.1:c.509A=	XP_016882076.1:p.Asp170=
XR_001753655.1:n.1096A=
XR_935791.2:n.1026A=
NM_000164.4:c.1001A= MANE Select	NP_000155.1:p.Asp334=
NM_001308418.2:c.893A=	NP_001295347.1:p.Asp298=