Canonical Allele Identifier: CA14677081
Gene: GIPR HGNC NCBI

Linked Data

dbSNP Id: rs11671664

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45669020G>A , CM000681.2:g.45669020G>A GRCh38
NC_000019.9:g.46172278G>A , CM000681.1:g.46172278G>A GRCh37
NC_000019.8:g.50864118G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000590918.6:c.-44-457G>A MANE Select ENSP00000467494.1:p.=
ENST00000652180.1:c.-359-295G>A ENSP00000498426.1:p.=
ENST00000263281.7:c.-44-457G>A ENSP00000263281.3:p.=
ENST00000304207.12:c.-44-457G>A ENSP00000305321.8:p.=
ENST00000585889.1:c.-44-457G>A ENSP00000467342.1:p.=
ENST00000590918.5:c.-44-457G>A ENSP00000467494.1:p.=
NM_000164.2:c.-44-457G>A NP_000155.1:p.=
NM_000164.3:c.-44-457G>A NP_000155.1:p.=
NM_001308418.1:c.-44-457G>A NP_001295347.1:p.=
XM_011526709.1:c.-44-457G>A XP_011525011.1:p.=
XM_011526710.1:c.-125-295G>A XP_011525012.1:p.=
XM_011526711.1:c.-44-457G>A XP_011525013.1:p.=
XM_011526712.1:c.-44-457G>A XP_011525014.1:p.=
XM_011526713.1:c.-44-457G>A XP_011525015.1:p.=
XM_011526714.1:c.-138+722G>A XP_011525016.1:p.=
XM_011526715.1:c.-148+722G>A XP_011525017.1:p.=
XM_011526716.1:c.-44-457G>A XP_011525018.1:p.=
XM_011526717.1:c.-44-457G>A XP_011525019.1:p.=
XM_011526709.2:c.-44-457G>A XP_011525011.1:p.=
XM_011526710.2:c.-125-295G>A XP_011525012.1:p.=
XM_011526711.2:c.-44-457G>A XP_011525013.1:p.=
XM_011526713.2:c.-44-457G>A XP_011525015.1:p.=
XM_011526714.2:c.-138+722G>A XP_011525016.1:p.=
XM_011526715.2:c.-148+722G>A XP_011525017.1:p.=
XM_011526716.2:c.-44-457G>A XP_011525018.1:p.=
NM_000164.4:c.-44-457G>A MANE Select NP_000155.1:p.=
NM_001308418.2:c.-44-457G>A NP_001295347.1:p.=