Canonical Allele Identifier: CA2338547515

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45669035_45669037delinsCAA , CM000681.2:g.45669035_45669037delinsCAA	GRCh38
NC_000019.9:g.46172293_46172295delinsCAA , CM000681.1:g.46172293_46172295delinsCAA	GRCh37
NC_000019.8:g.50864133_50864135delinsCAA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.-44-442_-44-440delinsCAA MANE Select	ENSP00000467494.1:n.-44-442_-44-440delins...
ENST00000652180.1:c.-359-280_-359-278delinsCAA	ENSP00000498426.1:n.-359-280_-359-278deli...
ENST00000263281.7:c.-44-442_-44-440delinsCAA	ENSP00000263281.3:n.-44-442_-44-440delins...
ENST00000304207.12:c.-44-442_-44-440delinsCAA	ENSP00000305321.8:n.-44-442_-44-440delins...
ENST00000585889.1:c.-44-442_-44-440delinsCAA	ENSP00000467342.1:n.-44-442_-44-440delins...
ENST00000590918.5:c.-44-442_-44-440delinsCAA	ENSP00000467494.1:n.-44-442_-44-440delins...
NM_000164.2:c.-44-442_-44-440delinsCAA	NP_000155.1:n.-44-442_-44-440delinsCAA
NM_000164.3:c.-44-442_-44-440delinsCAA	NP_000155.1:n.-44-442_-44-440delinsCAA
NM_001308418.1:c.-44-442_-44-440delinsCAA	NP_001295347.1:n.-44-442_-44-440delinsCAA...
XM_011526709.1:c.-44-442_-44-440delinsCAA	XP_011525011.1:n.-44-442_-44-440delinsCAA...
XM_011526710.1:c.-125-280_-125-278delinsCAA	XP_011525012.1:n.-125-280_-125-278delinsC...
XM_011526711.1:c.-44-442_-44-440delinsCAA	XP_011525013.1:n.-44-442_-44-440delinsCAA...
XM_011526712.1:c.-44-442_-44-440delinsCAA	XP_011525014.1:n.-44-442_-44-440delinsCAA...
XM_011526713.1:c.-44-442_-44-440delinsCAA	XP_011525015.1:n.-44-442_-44-440delinsCAA...
XM_011526714.1:c.-138+737_-138+739delinsCAA	XP_011525016.1:n.-138+737_-138+739delinsC...
XM_011526715.1:c.-148+737_-148+739delinsCAA	XP_011525017.1:n.-148+737_-148+739delinsC...
XM_011526716.1:c.-44-442_-44-440delinsCAA	XP_011525018.1:n.-44-442_-44-440delinsCAA...
XM_011526717.1:c.-44-442_-44-440delinsCAA	XP_011525019.1:n.-44-442_-44-440delinsCAA...
XR_935791.1:n.107-442_107-440delinsCAA
XM_011526709.2:c.-44-442_-44-440delinsCAA	XP_011525011.1:n.-44-442_-44-440delinsCAA...
XM_011526710.2:c.-125-280_-125-278delinsCAA	XP_011525012.1:n.-125-280_-125-278delinsC...
XM_011526711.2:c.-44-442_-44-440delinsCAA	XP_011525013.1:n.-44-442_-44-440delinsCAA...
XM_011526713.2:c.-44-442_-44-440delinsCAA	XP_011525015.1:n.-44-442_-44-440delinsCAA...
XM_011526714.2:c.-138+737_-138+739delinsCAA	XP_011525016.1:n.-138+737_-138+739delinsC...
XM_011526715.2:c.-148+737_-148+739delinsCAA	XP_011525017.1:n.-148+737_-148+739delinsC...
XM_011526716.2:c.-44-442_-44-440delinsCAA	XP_011525018.1:n.-44-442_-44-440delinsCAA...
XR_001753655.1:n.113-442_113-440delinsCAA
XR_935791.2:n.113-442_113-440delinsCAA
NM_000164.4:c.-44-442_-44-440delinsCAA MANE Select	NP_000155.1:n.-44-442_-44-440delinsCAA
NM_001308418.2:c.-44-442_-44-440delinsCAA	NP_001295347.1:n.-44-442_-44-440delinsCAA...