Canonical Allele Identifier: CA2338547462
Gene: GIPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45668903G= , CM000681.2:g.45668903G= GRCh38
NC_000019.9:g.46172161G= , CM000681.1:g.46172161G= GRCh37
NC_000019.8:g.50864001G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000590918.6:c.-44-574G= MANE Select ENSP00000467494.1:n.-44-574G=
ENST00000652180.1:c.-359-412G= ENSP00000498426.1:n.-359-412G=
ENST00000263281.7:c.-44-574G= ENSP00000263281.3:n.-44-574G=
ENST00000304207.12:c.-44-574G= ENSP00000305321.8:n.-44-574G=
ENST00000585889.1:c.-44-574G= ENSP00000467342.1:n.-44-574G=
ENST00000590918.5:c.-44-574G= ENSP00000467494.1:n.-44-574G=
NM_000164.2:c.-44-574G= NP_000155.1:n.-44-574G=
NM_000164.3:c.-44-574G= NP_000155.1:n.-44-574G=
NM_001308418.1:c.-44-574G= NP_001295347.1:n.-44-574G=
XM_011526709.1:c.-44-574G= XP_011525011.1:n.-44-574G=
XM_011526710.1:c.-125-412G= XP_011525012.1:n.-125-412G=
XM_011526711.1:c.-44-574G= XP_011525013.1:n.-44-574G=
XM_011526712.1:c.-44-574G= XP_011525014.1:n.-44-574G=
XM_011526713.1:c.-44-574G= XP_011525015.1:n.-44-574G=
XM_011526714.1:c.-138+605G= XP_011525016.1:n.-138+605G=
XM_011526715.1:c.-148+605G= XP_011525017.1:n.-148+605G=
XM_011526716.1:c.-44-574G= XP_011525018.1:n.-44-574G=
XM_011526717.1:c.-44-574G= XP_011525019.1:n.-44-574G=
XR_935791.1:n.107-574G=
XM_011526709.2:c.-44-574G= XP_011525011.1:n.-44-574G=
XM_011526710.2:c.-125-412G= XP_011525012.1:n.-125-412G=
XM_011526711.2:c.-44-574G= XP_011525013.1:n.-44-574G=
XM_011526713.2:c.-44-574G= XP_011525015.1:n.-44-574G=
XM_011526714.2:c.-138+605G= XP_011525016.1:n.-138+605G=
XM_011526715.2:c.-148+605G= XP_011525017.1:n.-148+605G=
XM_011526716.2:c.-44-574G= XP_011525018.1:n.-44-574G=
XR_001753655.1:n.113-574G=
XR_935791.2:n.113-574G=
NM_000164.4:c.-44-574G= MANE Select NP_000155.1:n.-44-574G=
NM_001308418.2:c.-44-574G= NP_001295347.1:n.-44-574G=