Canonical Allele Identifier: CA406395535

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181408C>A (hg19) ; chr19:g.45678150C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678150C>A , CM000681.2:g.45678150C>A	GRCh38
NC_000019.9:g.46181408C>A , CM000681.1:g.46181408C>A	GRCh37
NC_000019.8:g.50873248C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1076C>A MANE Select	ENSP00000467494.1:p.Pro359His
ENST00000652180.1:c.893C>A	ENSP00000498426.1:p.Pro298His
ENST00000263281.7:c.1076C>A	ENSP00000263281.3:p.Pro359His
ENST00000304207.12:c.968C>A	ENSP00000305321.8:p.Pro323His
ENST00000585889.1:c.*147C>A	ENSP00000467342.1:n.*147C>A
ENST00000590918.5:c.1076C>A	ENSP00000467494.1:p.Pro359His
ENST00000591224.1:n.532C>A
NM_000164.2:c.1076C>A	NP_000155.1:p.Pro359His
NM_000164.3:c.1076C>A	NP_000155.1:p.Pro359His
NM_001308418.1:c.968C>A	NP_001295347.1:p.Pro323His
XM_011526709.1:c.1202C>A	XP_011525011.1:p.Pro401His
XM_011526710.1:c.1202C>A	XP_011525012.1:p.Pro401His
XM_011526711.1:c.1094C>A	XP_011525013.1:p.Pro365His
XM_011526712.1:c.968C>A	XP_011525014.1:p.Pro323His
XM_011526713.1:c.953C>A	XP_011525015.1:p.Pro318His
XM_011526714.1:c.785C>A	XP_011525016.1:p.Pro262His
XM_011526715.1:c.785C>A	XP_011525017.1:p.Pro262His
XR_935791.1:n.1095C>A
XM_011526709.2:c.1202C>A	XP_011525011.1:p.Pro401His
XM_011526710.2:c.1202C>A	XP_011525012.1:p.Pro401His
XM_011526711.2:c.1094C>A	XP_011525013.1:p.Pro365His
XM_011526713.2:c.953C>A	XP_011525015.1:p.Pro318His
XM_011526714.2:c.785C>A	XP_011525016.1:p.Pro262His
XM_011526715.2:c.785C>A	XP_011525017.1:p.Pro262His
XM_017026584.1:c.731C>A	XP_016882073.1:p.Pro244His
XM_017026585.1:c.710C>A	XP_016882074.1:p.Pro237His
XM_017026586.1:c.587C>A	XP_016882075.1:p.Pro196His
XM_017026587.1:c.584C>A	XP_016882076.1:p.Pro195His
XR_001753655.1:n.1171C>A
XR_935791.2:n.1101C>A
NM_000164.4:c.1076C>A MANE Select	NP_000155.1:p.Pro359His
NM_001308418.2:c.968C>A	NP_001295347.1:p.Pro323His