Canonical Allele Identifier: CA406395072
Gene: GIPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45677937G>C , CM000681.2:g.45677937G>C GRCh38
NC_000019.9:g.46181195G>C , CM000681.1:g.46181195G>C GRCh37
NC_000019.8:g.50873035G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000590918.6:c.956G>C MANE Select ENSP00000467494.1:p.Gly319Ala
ENST00000652180.1:c.773G>C ENSP00000498426.1:p.Gly258Ala
ENST00000263281.7:c.956G>C ENSP00000263281.3:p.Gly319Ala
ENST00000304207.12:c.848G>C ENSP00000305321.8:p.Gly283Ala
ENST00000585889.1:c.*27G>C ENSP00000467342.1:n.*27G>C
ENST00000590918.5:c.956G>C ENSP00000467494.1:p.Gly319Ala
ENST00000591224.1:n.412G>C
ENST00000593127.1:n.57G>C
NM_000164.2:c.956G>C NP_000155.1:p.Gly319Ala
NM_000164.3:c.956G>C NP_000155.1:p.Gly319Ala
NM_001308418.1:c.848G>C NP_001295347.1:p.Gly283Ala
XM_011526709.1:c.1082G>C XP_011525011.1:p.Gly361Ala
XM_011526710.1:c.1082G>C XP_011525012.1:p.Gly361Ala
XM_011526711.1:c.974G>C XP_011525013.1:p.Gly325Ala
XM_011526712.1:c.848G>C XP_011525014.1:p.Gly283Ala
XM_011526713.1:c.833G>C XP_011525015.1:p.Gly278Ala
XM_011526714.1:c.665G>C XP_011525016.1:p.Gly222Ala
XM_011526715.1:c.665G>C XP_011525017.1:p.Gly222Ala
XM_011526716.1:c.*40G>C XP_011525018.1:n.*40G>C
XM_011526717.1:c.*40G>C XP_011525019.1:n.*40G>C
XR_935791.1:n.975G>C
XM_011526709.2:c.1082G>C XP_011525011.1:p.Gly361Ala
XM_011526710.2:c.1082G>C XP_011525012.1:p.Gly361Ala
XM_011526711.2:c.974G>C XP_011525013.1:p.Gly325Ala
XM_011526713.2:c.833G>C XP_011525015.1:p.Gly278Ala
XM_011526714.2:c.665G>C XP_011525016.1:p.Gly222Ala
XM_011526715.2:c.665G>C XP_011525017.1:p.Gly222Ala
XM_011526716.2:c.*40G>C XP_011525018.1:n.*40G>C
XM_017026584.1:c.611G>C XP_016882073.1:p.Gly204Ala
XM_017026585.1:c.590G>C XP_016882074.1:p.Gly197Ala
XM_017026586.1:c.467G>C XP_016882075.1:p.Gly156Ala
XM_017026587.1:c.464G>C XP_016882076.1:p.Gly155Ala
XR_001753655.1:n.1051G>C
XR_935791.2:n.981G>C
NM_000164.4:c.956G>C MANE Select NP_000155.1:p.Gly319Ala
NM_001308418.2:c.848G>C NP_001295347.1:p.Gly283Ala