Canonical Allele Identifier: CA2338552226
Gene: GIPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45678153T= , CM000681.2:g.45678153T= GRCh38
NC_000019.9:g.46181411T= , CM000681.1:g.46181411T= GRCh37
NC_000019.8:g.50873251T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000590918.6:c.1079T= MANE Select ENSP00000467494.1:p.Val360=
ENST00000652180.1:c.896T= ENSP00000498426.1:p.Val299=
ENST00000263281.7:c.1079T= ENSP00000263281.3:p.Val360=
ENST00000304207.12:c.971T= ENSP00000305321.8:p.Val324=
ENST00000585889.1:c.*150T= ENSP00000467342.1:n.*150T=
ENST00000590918.5:c.1079T= ENSP00000467494.1:p.Val360=
ENST00000591224.1:n.535T=
NM_000164.2:c.1079T= NP_000155.1:p.Val360=
NM_000164.3:c.1079T= NP_000155.1:p.Val360=
NM_001308418.1:c.971T= NP_001295347.1:p.Val324=
XM_011526709.1:c.1205T= XP_011525011.1:p.Val402=
XM_011526710.1:c.1205T= XP_011525012.1:p.Val402=
XM_011526711.1:c.1097T= XP_011525013.1:p.Val366=
XM_011526712.1:c.971T= XP_011525014.1:p.Val324=
XM_011526713.1:c.956T= XP_011525015.1:p.Val319=
XM_011526714.1:c.788T= XP_011525016.1:p.Val263=
XM_011526715.1:c.788T= XP_011525017.1:p.Val263=
XR_935791.1:n.1098T=
XM_011526709.2:c.1205T= XP_011525011.1:p.Val402=
XM_011526710.2:c.1205T= XP_011525012.1:p.Val402=
XM_011526711.2:c.1097T= XP_011525013.1:p.Val366=
XM_011526713.2:c.956T= XP_011525015.1:p.Val319=
XM_011526714.2:c.788T= XP_011525016.1:p.Val263=
XM_011526715.2:c.788T= XP_011525017.1:p.Val263=
XM_017026584.1:c.734T= XP_016882073.1:p.Val245=
XM_017026585.1:c.713T= XP_016882074.1:p.Val238=
XM_017026586.1:c.590T= XP_016882075.1:p.Val197=
XM_017026587.1:c.587T= XP_016882076.1:p.Val196=
XR_001753655.1:n.1174T=
XR_935791.2:n.1104T=
NM_000164.4:c.1079T= MANE Select NP_000155.1:p.Val360=
NM_001308418.2:c.971T= NP_001295347.1:p.Val324=