Canonical Allele Identifier: CA2338548652
Gene: GIPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45671129A= , CM000681.2:g.45671129A= GRCh38
NC_000019.9:g.46174387A= , CM000681.1:g.46174387A= GRCh37
NC_000019.8:g.50866227A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000590918.6:c.173-156A= MANE Select ENSP00000467494.1:n.173-156A=
ENST00000652180.1:c.-82+395A= ENSP00000498426.1:n.-82+395A=
ENST00000263281.7:c.173-156A= ENSP00000263281.3:n.173-156A=
ENST00000304207.12:c.172+395A= ENSP00000305321.8:n.172+395A=
ENST00000585889.1:c.173-156A= ENSP00000467342.1:n.173-156A=
ENST00000590918.5:c.173-156A= ENSP00000467494.1:n.173-156A=
ENST00000591322.1:c.-26-156A= ENSP00000465385.1:n.-26-156A=
NM_000164.2:c.173-156A= NP_000155.1:n.173-156A=
NM_000164.3:c.173-156A= NP_000155.1:n.173-156A=
NM_001308418.1:c.172+395A= NP_001295347.1:n.172+395A=
XM_011526709.1:c.173-156A= XP_011525011.1:n.173-156A=
XM_011526710.1:c.173-156A= XP_011525012.1:n.173-156A=
XM_011526711.1:c.172+395A= XP_011525013.1:n.172+395A=
XM_011526712.1:c.172+395A= XP_011525014.1:n.172+395A=
XM_011526713.1:c.173-156A= XP_011525015.1:n.173-156A=
XM_011526714.1:c.-137-1722A= XP_011525016.1:n.-137-1722A=
XM_011526715.1:c.-147-1722A= XP_011525017.1:n.-147-1722A=
XM_011526716.1:c.173-156A= XP_011525018.1:n.173-156A=
XM_011526717.1:c.173-156A= XP_011525019.1:n.173-156A=
XR_935791.1:n.323-156A=
XM_011526709.2:c.173-156A= XP_011525011.1:n.173-156A=
XM_011526710.2:c.173-156A= XP_011525012.1:n.173-156A=
XM_011526711.2:c.172+395A= XP_011525013.1:n.172+395A=
XM_011526713.2:c.173-156A= XP_011525015.1:n.173-156A=
XM_011526714.2:c.-137-1722A= XP_011525016.1:n.-137-1722A=
XM_011526715.2:c.-147-1722A= XP_011525017.1:n.-147-1722A=
XM_011526716.2:c.173-156A= XP_011525018.1:n.173-156A=
XR_001753655.1:n.329-156A=
XR_935791.2:n.329-156A=
NM_000164.4:c.173-156A= MANE Select NP_000155.1:n.173-156A=
NM_001308418.2:c.172+395A= NP_001295347.1:n.172+395A=