Canonical Allele Identifier: CA406395139

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181215A>G (hg19) ; chr19:g.45677957A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677957A>G , CM000681.2:g.45677957A>G	GRCh38
NC_000019.9:g.46181215A>G , CM000681.1:g.46181215A>G	GRCh37
NC_000019.8:g.50873055A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.976A>G MANE Select	ENSP00000467494.1:p.Arg326Gly
ENST00000652180.1:c.793A>G	ENSP00000498426.1:p.Arg265Gly
ENST00000263281.7:c.976A>G	ENSP00000263281.3:p.Arg326Gly
ENST00000304207.12:c.868A>G	ENSP00000305321.8:p.Arg290Gly
ENST00000585889.1:c.*47A>G	ENSP00000467342.1:n.*47A>G
ENST00000590918.5:c.976A>G	ENSP00000467494.1:p.Arg326Gly
ENST00000591224.1:n.432A>G
ENST00000593127.1:n.77A>G
NM_000164.2:c.976A>G	NP_000155.1:p.Arg326Gly
NM_000164.3:c.976A>G	NP_000155.1:p.Arg326Gly
NM_001308418.1:c.868A>G	NP_001295347.1:p.Arg290Gly
XM_011526709.1:c.1102A>G	XP_011525011.1:p.Arg368Gly
XM_011526710.1:c.1102A>G	XP_011525012.1:p.Arg368Gly
XM_011526711.1:c.994A>G	XP_011525013.1:p.Arg332Gly
XM_011526712.1:c.868A>G	XP_011525014.1:p.Arg290Gly
XM_011526713.1:c.853A>G	XP_011525015.1:p.Arg285Gly
XM_011526714.1:c.685A>G	XP_011525016.1:p.Arg229Gly
XM_011526715.1:c.685A>G	XP_011525017.1:p.Arg229Gly
XM_011526716.1:c.*60A>G	XP_011525018.1:n.*60A>G
XM_011526717.1:c.*60A>G	XP_011525019.1:n.*60A>G
XR_935791.1:n.995A>G
XM_011526709.2:c.1102A>G	XP_011525011.1:p.Arg368Gly
XM_011526710.2:c.1102A>G	XP_011525012.1:p.Arg368Gly
XM_011526711.2:c.994A>G	XP_011525013.1:p.Arg332Gly
XM_011526713.2:c.853A>G	XP_011525015.1:p.Arg285Gly
XM_011526714.2:c.685A>G	XP_011525016.1:p.Arg229Gly
XM_011526715.2:c.685A>G	XP_011525017.1:p.Arg229Gly
XM_011526716.2:c.*60A>G	XP_011525018.1:n.*60A>G
XM_017026584.1:c.631A>G	XP_016882073.1:p.Arg211Gly
XM_017026585.1:c.610A>G	XP_016882074.1:p.Arg204Gly
XM_017026586.1:c.487A>G	XP_016882075.1:p.Arg163Gly
XM_017026587.1:c.484A>G	XP_016882076.1:p.Arg162Gly
XR_001753655.1:n.1071A>G
XR_935791.2:n.1001A>G
NM_000164.4:c.976A>G MANE Select	NP_000155.1:p.Arg326Gly
NM_001308418.2:c.868A>G	NP_001295347.1:p.Arg290Gly