Canonical Allele Identifier: CA406395128
Gene: GIPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45677953G>C , CM000681.2:g.45677953G>C GRCh38
NC_000019.9:g.46181211G>C , CM000681.1:g.46181211G>C GRCh37
NC_000019.8:g.50873051G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000590918.6:c.972G>C MANE Select ENSP00000467494.1:p.Lys324Asn
ENST00000652180.1:c.789G>C ENSP00000498426.1:p.Lys263Asn
ENST00000263281.7:c.972G>C ENSP00000263281.3:p.Lys324Asn
ENST00000304207.12:c.864G>C ENSP00000305321.8:p.Lys288Asn
ENST00000585889.1:c.*43G>C ENSP00000467342.1:n.*43G>C
ENST00000590918.5:c.972G>C ENSP00000467494.1:p.Lys324Asn
ENST00000591224.1:n.428G>C
ENST00000593127.1:n.73G>C
NM_000164.2:c.972G>C NP_000155.1:p.Lys324Asn
NM_000164.3:c.972G>C NP_000155.1:p.Lys324Asn
NM_001308418.1:c.864G>C NP_001295347.1:p.Lys288Asn
XM_011526709.1:c.1098G>C XP_011525011.1:p.Lys366Asn
XM_011526710.1:c.1098G>C XP_011525012.1:p.Lys366Asn
XM_011526711.1:c.990G>C XP_011525013.1:p.Lys330Asn
XM_011526712.1:c.864G>C XP_011525014.1:p.Lys288Asn
XM_011526713.1:c.849G>C XP_011525015.1:p.Lys283Asn
XM_011526714.1:c.681G>C XP_011525016.1:p.Lys227Asn
XM_011526715.1:c.681G>C XP_011525017.1:p.Lys227Asn
XM_011526716.1:c.*56G>C XP_011525018.1:n.*56G>C
XM_011526717.1:c.*56G>C XP_011525019.1:n.*56G>C
XR_935791.1:n.991G>C
XM_011526709.2:c.1098G>C XP_011525011.1:p.Lys366Asn
XM_011526710.2:c.1098G>C XP_011525012.1:p.Lys366Asn
XM_011526711.2:c.990G>C XP_011525013.1:p.Lys330Asn
XM_011526713.2:c.849G>C XP_011525015.1:p.Lys283Asn
XM_011526714.2:c.681G>C XP_011525016.1:p.Lys227Asn
XM_011526715.2:c.681G>C XP_011525017.1:p.Lys227Asn
XM_011526716.2:c.*56G>C XP_011525018.1:n.*56G>C
XM_017026584.1:c.627G>C XP_016882073.1:p.Lys209Asn
XM_017026585.1:c.606G>C XP_016882074.1:p.Lys202Asn
XM_017026586.1:c.483G>C XP_016882075.1:p.Lys161Asn
XM_017026587.1:c.480G>C XP_016882076.1:p.Lys160Asn
XR_001753655.1:n.1067G>C
XR_935791.2:n.997G>C
NM_000164.4:c.972G>C MANE Select NP_000155.1:p.Lys324Asn
NM_001308418.2:c.864G>C NP_001295347.1:p.Lys288Asn