Canonical Allele Identifier: CA2338547526

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45669054T= , CM000681.2:g.45669054T=	GRCh38
NC_000019.9:g.46172312T= , CM000681.1:g.46172312T=	GRCh37
NC_000019.8:g.50864152T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.-44-423T= MANE Select	ENSP00000467494.1:n.-44-423T=
ENST00000652180.1:c.-359-261T=	ENSP00000498426.1:n.-359-261T=
ENST00000263281.7:c.-44-423T=	ENSP00000263281.3:n.-44-423T=
ENST00000304207.12:c.-44-423T=	ENSP00000305321.8:n.-44-423T=
ENST00000585889.1:c.-44-423T=	ENSP00000467342.1:n.-44-423T=
ENST00000590918.5:c.-44-423T=	ENSP00000467494.1:n.-44-423T=
NM_000164.2:c.-44-423T=	NP_000155.1:n.-44-423T=
NM_000164.3:c.-44-423T=	NP_000155.1:n.-44-423T=
NM_001308418.1:c.-44-423T=	NP_001295347.1:n.-44-423T=
XM_011526709.1:c.-44-423T=	XP_011525011.1:n.-44-423T=
XM_011526710.1:c.-125-261T=	XP_011525012.1:n.-125-261T=
XM_011526711.1:c.-44-423T=	XP_011525013.1:n.-44-423T=
XM_011526712.1:c.-44-423T=	XP_011525014.1:n.-44-423T=
XM_011526713.1:c.-44-423T=	XP_011525015.1:n.-44-423T=
XM_011526714.1:c.-138+756T=	XP_011525016.1:n.-138+756T=
XM_011526715.1:c.-148+756T=	XP_011525017.1:n.-148+756T=
XM_011526716.1:c.-44-423T=	XP_011525018.1:n.-44-423T=
XM_011526717.1:c.-44-423T=	XP_011525019.1:n.-44-423T=
XR_935791.1:n.107-423T=
XM_011526709.2:c.-44-423T=	XP_011525011.1:n.-44-423T=
XM_011526710.2:c.-125-261T=	XP_011525012.1:n.-125-261T=
XM_011526711.2:c.-44-423T=	XP_011525013.1:n.-44-423T=
XM_011526713.2:c.-44-423T=	XP_011525015.1:n.-44-423T=
XM_011526714.2:c.-138+756T=	XP_011525016.1:n.-138+756T=
XM_011526715.2:c.-148+756T=	XP_011525017.1:n.-148+756T=
XM_011526716.2:c.-44-423T=	XP_011525018.1:n.-44-423T=
XR_001753655.1:n.113-423T=
XR_935791.2:n.113-423T=
NM_000164.4:c.-44-423T= MANE Select	NP_000155.1:n.-44-423T=
NM_001308418.2:c.-44-423T=	NP_001295347.1:n.-44-423T=