Canonical Allele Identifier: CA507825136

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181238G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677980G>T , CM000681.2:g.45677980G>T	GRCh38
NC_000019.9:g.46181238G>T , CM000681.1:g.46181238G>T	GRCh37
NC_000019.8:g.50873078G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.999G>T MANE Select	ENSP00000467494.1:p.Arg333=
ENST00000652180.1:c.816G>T	ENSP00000498426.1:p.Arg272=
ENST00000263281.7:c.999G>T	ENSP00000263281.3:p.Arg333=
ENST00000304207.12:c.891G>T	ENSP00000305321.8:p.Arg297=
ENST00000585889.1:c.*70G>T	ENSP00000467342.1:n.*70G>T
ENST00000590918.5:c.999G>T	ENSP00000467494.1:p.Arg333=
ENST00000591224.1:n.455G>T
ENST00000593127.1:n.100G>T
NM_000164.2:c.999G>T	NP_000155.1:p.Arg333=
NM_000164.3:c.999G>T	NP_000155.1:p.Arg333=
NM_001308418.1:c.891G>T	NP_001295347.1:p.Arg297=
XM_011526709.1:c.1125G>T	XP_011525011.1:p.Arg375=
XM_011526710.1:c.1125G>T	XP_011525012.1:p.Arg375=
XM_011526711.1:c.1017G>T	XP_011525013.1:p.Arg339=
XM_011526712.1:c.891G>T	XP_011525014.1:p.Arg297=
XM_011526713.1:c.876G>T	XP_011525015.1:p.Arg292=
XM_011526714.1:c.708G>T	XP_011525016.1:p.Arg236=
XM_011526715.1:c.708G>T	XP_011525017.1:p.Arg236=
XM_011526716.1:c.*83G>T	XP_011525018.1:n.*83G>T
XM_011526717.1:c.*83G>T	XP_011525019.1:n.*83G>T
XR_935791.1:n.1018G>T
XM_011526709.2:c.1125G>T	XP_011525011.1:p.Arg375=
XM_011526710.2:c.1125G>T	XP_011525012.1:p.Arg375=
XM_011526711.2:c.1017G>T	XP_011525013.1:p.Arg339=
XM_011526713.2:c.876G>T	XP_011525015.1:p.Arg292=
XM_011526714.2:c.708G>T	XP_011525016.1:p.Arg236=
XM_011526715.2:c.708G>T	XP_011525017.1:p.Arg236=
XM_011526716.2:c.*83G>T	XP_011525018.1:n.*83G>T
XM_017026584.1:c.654G>T	XP_016882073.1:p.Arg218=
XM_017026585.1:c.633G>T	XP_016882074.1:p.Arg211=
XM_017026586.1:c.510G>T	XP_016882075.1:p.Arg170=
XM_017026587.1:c.507G>T	XP_016882076.1:p.Arg169=
XR_001753655.1:n.1094G>T
XR_935791.2:n.1024G>T
NM_000164.4:c.999G>T MANE Select	NP_000155.1:p.Arg333=
NM_001308418.2:c.891G>T	NP_001295347.1:p.Arg297=