Canonical Allele Identifier: CA14677083
Gene: GIPR HGNC NCBI

Linked Data

dbSNP Id: rs10423928

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45679046T>A , CM000681.2:g.45679046T>A GRCh38
NC_000019.9:g.46182304T>A , CM000681.1:g.46182304T>A GRCh37
NC_000019.8:g.50874144T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000590918.6:c.1152+820T>A MANE Select ENSP00000467494.1:p.=
ENST00000652180.1:c.969+820T>A ENSP00000498426.1:p.=
ENST00000263281.7:c.1152+820T>A ENSP00000263281.3:p.=
ENST00000304207.12:c.1044+820T>A ENSP00000305321.8:p.=
ENST00000585889.1:c.*223+820T>A ENSP00000467342.1:p.=
ENST00000590918.5:c.1152+820T>A ENSP00000467494.1:p.=
NM_000164.2:c.1152+820T>A NP_000155.1:p.=
NM_000164.3:c.1152+820T>A NP_000155.1:p.=
NM_001308418.1:c.1044+820T>A NP_001295347.1:p.=
XM_011526709.1:c.1278+820T>A XP_011525011.1:p.=
XM_011526710.1:c.1278+820T>A XP_011525012.1:p.=
XM_011526711.1:c.1170+820T>A XP_011525013.1:p.=
XM_011526712.1:c.1044+820T>A XP_011525014.1:p.=
XM_011526713.1:c.1029+820T>A XP_011525015.1:p.=
XM_011526714.1:c.861+820T>A XP_011525016.1:p.=
XM_011526715.1:c.861+820T>A XP_011525017.1:p.=
XM_011526709.2:c.1278+820T>A XP_011525011.1:p.=
XM_011526710.2:c.1278+820T>A XP_011525012.1:p.=
XM_011526711.2:c.1170+820T>A XP_011525013.1:p.=
XM_011526713.2:c.1029+820T>A XP_011525015.1:p.=
XM_011526714.2:c.861+820T>A XP_011525016.1:p.=
XM_011526715.2:c.861+820T>A XP_011525017.1:p.=
XM_017026584.1:c.807+820T>A XP_016882073.1:p.=
XM_017026585.1:c.786+820T>A XP_016882074.1:p.=
XM_017026586.1:c.663+820T>A XP_016882075.1:p.=
XM_017026587.1:c.660+820T>A XP_016882076.1:p.=
NM_000164.4:c.1152+820T>A MANE Select NP_000155.1:p.=
NM_001308418.2:c.1044+820T>A NP_001295347.1:p.=