Canonical Allele Identifier: CA507825130
Gene: GIPR HGNC NCBI

Linked Data

dbSNP Id: rs1967044231
MyVariant Identifiers: chr19:g.46181232C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45677974C>T , CM000681.2:g.45677974C>T GRCh38
NC_000019.9:g.46181232C>T , CM000681.1:g.46181232C>T GRCh37
NC_000019.8:g.50873072C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000590918.6:c.993C>T MANE Select ENSP00000467494.1:p.Arg331=
ENST00000652180.1:c.810C>T ENSP00000498426.1:p.Arg270=
ENST00000263281.7:c.993C>T ENSP00000263281.3:p.Arg331=
ENST00000304207.12:c.885C>T ENSP00000305321.8:p.Arg295=
ENST00000585889.1:c.*64C>T ENSP00000467342.1:n.*64C>T
ENST00000590918.5:c.993C>T ENSP00000467494.1:p.Arg331=
ENST00000591224.1:n.449C>T
ENST00000593127.1:n.94C>T
NM_000164.2:c.993C>T NP_000155.1:p.Arg331=
NM_000164.3:c.993C>T NP_000155.1:p.Arg331=
NM_001308418.1:c.885C>T NP_001295347.1:p.Arg295=
XM_011526709.1:c.1119C>T XP_011525011.1:p.Arg373=
XM_011526710.1:c.1119C>T XP_011525012.1:p.Arg373=
XM_011526711.1:c.1011C>T XP_011525013.1:p.Arg337=
XM_011526712.1:c.885C>T XP_011525014.1:p.Arg295=
XM_011526713.1:c.870C>T XP_011525015.1:p.Arg290=
XM_011526714.1:c.702C>T XP_011525016.1:p.Arg234=
XM_011526715.1:c.702C>T XP_011525017.1:p.Arg234=
XM_011526716.1:c.*77C>T XP_011525018.1:n.*77C>T
XM_011526717.1:c.*77C>T XP_011525019.1:n.*77C>T
XR_935791.1:n.1012C>T
XM_011526709.2:c.1119C>T XP_011525011.1:p.Arg373=
XM_011526710.2:c.1119C>T XP_011525012.1:p.Arg373=
XM_011526711.2:c.1011C>T XP_011525013.1:p.Arg337=
XM_011526713.2:c.870C>T XP_011525015.1:p.Arg290=
XM_011526714.2:c.702C>T XP_011525016.1:p.Arg234=
XM_011526715.2:c.702C>T XP_011525017.1:p.Arg234=
XM_011526716.2:c.*77C>T XP_011525018.1:n.*77C>T
XM_017026584.1:c.648C>T XP_016882073.1:p.Arg216=
XM_017026585.1:c.627C>T XP_016882074.1:p.Arg209=
XM_017026586.1:c.504C>T XP_016882075.1:p.Arg168=
XM_017026587.1:c.501C>T XP_016882076.1:p.Arg167=
XR_001753655.1:n.1088C>T
XR_935791.2:n.1018C>T
NM_000164.4:c.993C>T MANE Select NP_000155.1:p.Arg331=
NM_001308418.2:c.885C>T NP_001295347.1:p.Arg295=