Canonical Allele Identifier: CA9519198
Gene: GIPR HGNC NCBI

Linked Data

dbSNP Id: rs1800437

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45678134G>C , CM000681.2:g.45678134G>C GRCh38
NC_000019.9:g.46181392G>C , CM000681.1:g.46181392G>C GRCh37
NC_000019.8:g.50873232G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000590918.6:c.1060G>C MANE Select ENSP00000467494.1:p.Glu354Gln
ENST00000652180.1:c.877G>C ENSP00000498426.1:p.Glu293Gln
ENST00000263281.7:c.1060G>C ENSP00000263281.3:p.Glu354Gln
ENST00000304207.12:c.952G>C ENSP00000305321.8:p.Glu318Gln
ENST00000585889.1:c.*131G>C ENSP00000467342.1:p.=
ENST00000590918.5:c.1060G>C ENSP00000467494.1:p.Glu354Gln
NM_000164.2:c.1060G>C NP_000155.1:p.Glu354Gln
NM_000164.3:c.1060G>C NP_000155.1:p.Glu354Gln
NM_001308418.1:c.952G>C NP_001295347.1:p.Glu318Gln
XM_011526709.1:c.1186G>C XP_011525011.1:p.Glu396Gln
XM_011526710.1:c.1186G>C XP_011525012.1:p.Glu396Gln
XM_011526711.1:c.1078G>C XP_011525013.1:p.Glu360Gln
XM_011526712.1:c.952G>C XP_011525014.1:p.Glu318Gln
XM_011526713.1:c.937G>C XP_011525015.1:p.Glu313Gln
XM_011526714.1:c.769G>C XP_011525016.1:p.Glu257Gln
XM_011526715.1:c.769G>C XP_011525017.1:p.Glu257Gln
XM_011526709.2:c.1186G>C XP_011525011.1:p.Glu396Gln
XM_011526710.2:c.1186G>C XP_011525012.1:p.Glu396Gln
XM_011526711.2:c.1078G>C XP_011525013.1:p.Glu360Gln
XM_011526713.2:c.937G>C XP_011525015.1:p.Glu313Gln
XM_011526714.2:c.769G>C XP_011525016.1:p.Glu257Gln
XM_011526715.2:c.769G>C XP_011525017.1:p.Glu257Gln
XM_017026584.1:c.715G>C XP_016882073.1:p.Glu239Gln
XM_017026585.1:c.694G>C XP_016882074.1:p.Glu232Gln
XM_017026586.1:c.571G>C XP_016882075.1:p.Glu191Gln
XM_017026587.1:c.568G>C XP_016882076.1:p.Glu190Gln
NM_000164.4:c.1060G>C MANE Select NP_000155.1:p.Glu354Gln
NM_001308418.2:c.952G>C NP_001295347.1:p.Glu318Gln