Canonical Allele Identifier: CA2585842739
Gene: GIPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45678078C>A , CM000681.2:g.45678078C>A GRCh38
NC_000019.9:g.46181336C>A , CM000681.1:g.46181336C>A GRCh37
NC_000019.8:g.50873176C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000590918.6:c.1014-10C>A MANE Select ENSP00000467494.1:n.1014-10C>A
ENST00000652180.1:c.831-10C>A ENSP00000498426.1:n.831-10C>A
ENST00000263281.7:c.1014-10C>A ENSP00000263281.3:n.1014-10C>A
ENST00000304207.12:c.906-10C>A ENSP00000305321.8:n.906-10C>A
ENST00000585889.1:c.*85-10C>A ENSP00000467342.1:n.*85-10C>A
ENST00000590918.5:c.1014-10C>A ENSP00000467494.1:n.1014-10C>A
ENST00000591224.1:n.470-10C>A
ENST00000593127.1:n.115-10C>A
NM_000164.2:c.1014-10C>A NP_000155.1:n.1014-10C>A
NM_000164.3:c.1014-10C>A NP_000155.1:n.1014-10C>A
NM_001308418.1:c.906-10C>A NP_001295347.1:n.906-10C>A
XM_011526709.1:c.1140-10C>A XP_011525011.1:n.1140-10C>A
XM_011526710.1:c.1140-10C>A XP_011525012.1:n.1140-10C>A
XM_011526711.1:c.1032-10C>A XP_011525013.1:n.1032-10C>A
XM_011526712.1:c.906-10C>A XP_011525014.1:n.906-10C>A
XM_011526713.1:c.891-10C>A XP_011525015.1:n.891-10C>A
XM_011526714.1:c.723-10C>A XP_011525016.1:n.723-10C>A
XM_011526715.1:c.723-10C>A XP_011525017.1:n.723-10C>A
XR_935791.1:n.1033-10C>A
XM_011526709.2:c.1140-10C>A XP_011525011.1:n.1140-10C>A
XM_011526710.2:c.1140-10C>A XP_011525012.1:n.1140-10C>A
XM_011526711.2:c.1032-10C>A XP_011525013.1:n.1032-10C>A
XM_011526713.2:c.891-10C>A XP_011525015.1:n.891-10C>A
XM_011526714.2:c.723-10C>A XP_011525016.1:n.723-10C>A
XM_011526715.2:c.723-10C>A XP_011525017.1:n.723-10C>A
XM_017026584.1:c.669-10C>A XP_016882073.1:n.669-10C>A
XM_017026585.1:c.648-10C>A XP_016882074.1:n.648-10C>A
XM_017026586.1:c.525-10C>A XP_016882075.1:n.525-10C>A
XM_017026587.1:c.522-10C>A XP_016882076.1:n.522-10C>A
XR_001753655.1:n.1109-10C>A
XR_935791.2:n.1039-10C>A
NM_000164.4:c.1014-10C>A MANE Select NP_000155.1:n.1014-10C>A
NM_001308418.2:c.906-10C>A NP_001295347.1:n.906-10C>A