Canonical Allele Identifier: CA406395532

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181407C>G (hg19) ; chr19:g.45678149C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678149C>G , CM000681.2:g.45678149C>G	GRCh38
NC_000019.9:g.46181407C>G , CM000681.1:g.46181407C>G	GRCh37
NC_000019.8:g.50873247C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1075C>G MANE Select	ENSP00000467494.1:p.Pro359Ala
ENST00000652180.1:c.892C>G	ENSP00000498426.1:p.Pro298Ala
ENST00000263281.7:c.1075C>G	ENSP00000263281.3:p.Pro359Ala
ENST00000304207.12:c.967C>G	ENSP00000305321.8:p.Pro323Ala
ENST00000585889.1:c.*146C>G	ENSP00000467342.1:n.*146C>G
ENST00000590918.5:c.1075C>G	ENSP00000467494.1:p.Pro359Ala
ENST00000591224.1:n.531C>G
NM_000164.2:c.1075C>G	NP_000155.1:p.Pro359Ala
NM_000164.3:c.1075C>G	NP_000155.1:p.Pro359Ala
NM_001308418.1:c.967C>G	NP_001295347.1:p.Pro323Ala
XM_011526709.1:c.1201C>G	XP_011525011.1:p.Pro401Ala
XM_011526710.1:c.1201C>G	XP_011525012.1:p.Pro401Ala
XM_011526711.1:c.1093C>G	XP_011525013.1:p.Pro365Ala
XM_011526712.1:c.967C>G	XP_011525014.1:p.Pro323Ala
XM_011526713.1:c.952C>G	XP_011525015.1:p.Pro318Ala
XM_011526714.1:c.784C>G	XP_011525016.1:p.Pro262Ala
XM_011526715.1:c.784C>G	XP_011525017.1:p.Pro262Ala
XR_935791.1:n.1094C>G
XM_011526709.2:c.1201C>G	XP_011525011.1:p.Pro401Ala
XM_011526710.2:c.1201C>G	XP_011525012.1:p.Pro401Ala
XM_011526711.2:c.1093C>G	XP_011525013.1:p.Pro365Ala
XM_011526713.2:c.952C>G	XP_011525015.1:p.Pro318Ala
XM_011526714.2:c.784C>G	XP_011525016.1:p.Pro262Ala
XM_011526715.2:c.784C>G	XP_011525017.1:p.Pro262Ala
XM_017026584.1:c.730C>G	XP_016882073.1:p.Pro244Ala
XM_017026585.1:c.709C>G	XP_016882074.1:p.Pro237Ala
XM_017026586.1:c.586C>G	XP_016882075.1:p.Pro196Ala
XM_017026587.1:c.583C>G	XP_016882076.1:p.Pro195Ala
XR_001753655.1:n.1170C>G
XR_935791.2:n.1100C>G
NM_000164.4:c.1075C>G MANE Select	NP_000155.1:p.Pro359Ala
NM_001308418.2:c.967C>G	NP_001295347.1:p.Pro323Ala