Canonical Allele Identifier: CA308982203
Gene: GIPR HGNC NCBI

Linked Data

dbSNP Id: rs13306401

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45671120C>A , CM000681.2:g.45671120C>A GRCh38
NC_000019.9:g.46174378C>A , CM000681.1:g.46174378C>A GRCh37
NC_000019.8:g.50866218C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000590918.6:c.173-165C>A MANE Select ENSP00000467494.1:p.=
ENST00000652180.1:c.-82+386C>A ENSP00000498426.1:p.=
ENST00000263281.7:c.173-165C>A ENSP00000263281.3:p.=
ENST00000304207.12:c.172+386C>A ENSP00000305321.8:p.=
ENST00000585889.1:c.173-165C>A ENSP00000467342.1:p.=
ENST00000590918.5:c.173-165C>A ENSP00000467494.1:p.=
ENST00000591322.1:c.-26-165C>A ENSP00000465385.1:p.=
NM_000164.2:c.173-165C>A NP_000155.1:p.=
NM_000164.3:c.173-165C>A NP_000155.1:p.=
NM_001308418.1:c.172+386C>A NP_001295347.1:p.=
XM_011526709.1:c.173-165C>A XP_011525011.1:p.=
XM_011526710.1:c.173-165C>A XP_011525012.1:p.=
XM_011526711.1:c.172+386C>A XP_011525013.1:p.=
XM_011526712.1:c.172+386C>A XP_011525014.1:p.=
XM_011526713.1:c.173-165C>A XP_011525015.1:p.=
XM_011526714.1:c.-137-1731C>A XP_011525016.1:p.=
XM_011526715.1:c.-147-1731C>A XP_011525017.1:p.=
XM_011526716.1:c.173-165C>A XP_011525018.1:p.=
XM_011526717.1:c.173-165C>A XP_011525019.1:p.=
XR_935791.1:n.323-165C>A
XM_011526709.2:c.173-165C>A XP_011525011.1:p.=
XM_011526710.2:c.173-165C>A XP_011525012.1:p.=
XM_011526711.2:c.172+386C>A XP_011525013.1:p.=
XM_011526713.2:c.173-165C>A XP_011525015.1:p.=
XM_011526714.2:c.-137-1731C>A XP_011525016.1:p.=
XM_011526715.2:c.-147-1731C>A XP_011525017.1:p.=
XM_011526716.2:c.173-165C>A XP_011525018.1:p.=
XR_001753655.1:n.329-165C>A
XR_935791.2:n.329-165C>A
NM_000164.4:c.173-165C>A MANE Select NP_000155.1:p.=
NM_001308418.2:c.172+386C>A NP_001295347.1:p.=