Canonical Allele Identifier: CA2338547494

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45668975C= , CM000681.2:g.45668975C=	GRCh38
NC_000019.9:g.46172233C= , CM000681.1:g.46172233C=	GRCh37
NC_000019.8:g.50864073C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.-44-502C= MANE Select	ENSP00000467494.1:n.-44-502C=
ENST00000652180.1:c.-359-340C=	ENSP00000498426.1:n.-359-340C=
ENST00000263281.7:c.-44-502C=	ENSP00000263281.3:n.-44-502C=
ENST00000304207.12:c.-44-502C=	ENSP00000305321.8:n.-44-502C=
ENST00000585889.1:c.-44-502C=	ENSP00000467342.1:n.-44-502C=
ENST00000590918.5:c.-44-502C=	ENSP00000467494.1:n.-44-502C=
NM_000164.2:c.-44-502C=	NP_000155.1:n.-44-502C=
NM_000164.3:c.-44-502C=	NP_000155.1:n.-44-502C=
NM_001308418.1:c.-44-502C=	NP_001295347.1:n.-44-502C=
XM_011526709.1:c.-44-502C=	XP_011525011.1:n.-44-502C=
XM_011526710.1:c.-125-340C=	XP_011525012.1:n.-125-340C=
XM_011526711.1:c.-44-502C=	XP_011525013.1:n.-44-502C=
XM_011526712.1:c.-44-502C=	XP_011525014.1:n.-44-502C=
XM_011526713.1:c.-44-502C=	XP_011525015.1:n.-44-502C=
XM_011526714.1:c.-138+677C=	XP_011525016.1:n.-138+677C=
XM_011526715.1:c.-148+677C=	XP_011525017.1:n.-148+677C=
XM_011526716.1:c.-44-502C=	XP_011525018.1:n.-44-502C=
XM_011526717.1:c.-44-502C=	XP_011525019.1:n.-44-502C=
XR_935791.1:n.107-502C=
XM_011526709.2:c.-44-502C=	XP_011525011.1:n.-44-502C=
XM_011526710.2:c.-125-340C=	XP_011525012.1:n.-125-340C=
XM_011526711.2:c.-44-502C=	XP_011525013.1:n.-44-502C=
XM_011526713.2:c.-44-502C=	XP_011525015.1:n.-44-502C=
XM_011526714.2:c.-138+677C=	XP_011525016.1:n.-138+677C=
XM_011526715.2:c.-148+677C=	XP_011525017.1:n.-148+677C=
XM_011526716.2:c.-44-502C=	XP_011525018.1:n.-44-502C=
XR_001753655.1:n.113-502C=
XR_935791.2:n.113-502C=
NM_000164.4:c.-44-502C= MANE Select	NP_000155.1:n.-44-502C=
NM_001308418.2:c.-44-502C=	NP_001295347.1:n.-44-502C=