Canonical Allele Identifier: CA406395533

Gene: GIPR

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1075C>T MANE Select	ENSP00000467494.1:p.Pro359Ser
ENST00000652180.1:c.892C>T	ENSP00000498426.1:p.Pro298Ser
ENST00000263281.7:c.1075C>T	ENSP00000263281.3:p.Pro359Ser
ENST00000304207.12:c.967C>T	ENSP00000305321.8:p.Pro323Ser
ENST00000585889.1:c.*146C>T	ENSP00000467342.1:n.*146C>T
ENST00000590918.5:c.1075C>T	ENSP00000467494.1:p.Pro359Ser
ENST00000591224.1:n.531C>T
NM_000164.2:c.1075C>T	NP_000155.1:p.Pro359Ser
NM_000164.3:c.1075C>T	NP_000155.1:p.Pro359Ser
NM_001308418.1:c.967C>T	NP_001295347.1:p.Pro323Ser
XM_011526709.1:c.1201C>T	XP_011525011.1:p.Pro401Ser
XM_011526710.1:c.1201C>T	XP_011525012.1:p.Pro401Ser
XM_011526711.1:c.1093C>T	XP_011525013.1:p.Pro365Ser
XM_011526712.1:c.967C>T	XP_011525014.1:p.Pro323Ser
XM_011526713.1:c.952C>T	XP_011525015.1:p.Pro318Ser
XM_011526714.1:c.784C>T	XP_011525016.1:p.Pro262Ser
XM_011526715.1:c.784C>T	XP_011525017.1:p.Pro262Ser
XR_935791.1:n.1094C>T
XM_011526709.2:c.1201C>T	XP_011525011.1:p.Pro401Ser
XM_011526710.2:c.1201C>T	XP_011525012.1:p.Pro401Ser
XM_011526711.2:c.1093C>T	XP_011525013.1:p.Pro365Ser
XM_011526713.2:c.952C>T	XP_011525015.1:p.Pro318Ser
XM_011526714.2:c.784C>T	XP_011525016.1:p.Pro262Ser
XM_011526715.2:c.784C>T	XP_011525017.1:p.Pro262Ser
XM_017026584.1:c.730C>T	XP_016882073.1:p.Pro244Ser
XM_017026585.1:c.709C>T	XP_016882074.1:p.Pro237Ser
XM_017026586.1:c.586C>T	XP_016882075.1:p.Pro196Ser
XM_017026587.1:c.583C>T	XP_016882076.1:p.Pro195Ser
XR_001753655.1:n.1170C>T
XR_935791.2:n.1100C>T
NM_000164.4:c.1075C>T MANE Select	NP_000155.1:p.Pro359Ser
NM_001308418.2:c.967C>T	NP_001295347.1:p.Pro323Ser