Canonical Allele Identifier: CA633341531
Gene: GIPR HGNC NCBI

Linked Data

dbSNP Id: rs1296870463

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45669012del , CM000681.2:g.45669012del GRCh38
NC_000019.9:g.46172270del , CM000681.1:g.46172270del GRCh37
NC_000019.8:g.50864110del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000590918.6:c.-44-465del MANE Select ENSP00000467494.1:n.-44-465del
ENST00000652180.1:c.-359-303del ENSP00000498426.1:n.-359-303del
ENST00000263281.7:c.-44-465del ENSP00000263281.3:n.-44-465del
ENST00000304207.12:c.-44-465del ENSP00000305321.8:n.-44-465del
ENST00000585889.1:c.-44-465del ENSP00000467342.1:n.-44-465del
ENST00000590918.5:c.-44-465del ENSP00000467494.1:n.-44-465del
NM_000164.2:c.-44-465del NP_000155.1:n.-44-465del
NM_000164.3:c.-44-465del NP_000155.1:n.-44-465del
NM_001308418.1:c.-44-465del NP_001295347.1:n.-44-465del
XM_011526709.1:c.-44-465del XP_011525011.1:n.-44-465del
XM_011526710.1:c.-125-303del XP_011525012.1:n.-125-303del
XM_011526711.1:c.-44-465del XP_011525013.1:n.-44-465del
XM_011526712.1:c.-44-465del XP_011525014.1:n.-44-465del
XM_011526713.1:c.-44-465del XP_011525015.1:n.-44-465del
XM_011526714.1:c.-138+714del XP_011525016.1:n.-138+714del
XM_011526715.1:c.-148+714del XP_011525017.1:n.-148+714del
XM_011526716.1:c.-44-465del XP_011525018.1:n.-44-465del
XM_011526717.1:c.-44-465del XP_011525019.1:n.-44-465del
XR_935791.1:n.107-465del
XM_011526709.2:c.-44-465del XP_011525011.1:n.-44-465del
XM_011526710.2:c.-125-303del XP_011525012.1:n.-125-303del
XM_011526711.2:c.-44-465del XP_011525013.1:n.-44-465del
XM_011526713.2:c.-44-465del XP_011525015.1:n.-44-465del
XM_011526714.2:c.-138+714del XP_011525016.1:n.-138+714del
XM_011526715.2:c.-148+714del XP_011525017.1:n.-148+714del
XM_011526716.2:c.-44-465del XP_011525018.1:n.-44-465del
XR_001753655.1:n.113-465del
XR_935791.2:n.113-465del
NM_000164.4:c.-44-465del MANE Select NP_000155.1:n.-44-465del
NM_001308418.2:c.-44-465del NP_001295347.1:n.-44-465del