Canonical Allele Identifier: CA406395225

Gene: GIPR

Linked Data

• dbSNP Id: rs1335419201
• gnomAD v2: 19-46181237-G-A
• gnomAD v4: 19-45677979-G-A
• MyVariant Identifiers: chr19:g.46181237G>A (hg19) ; chr19:g.45677979G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677979G>A , CM000681.2:g.45677979G>A	GRCh38
NC_000019.9:g.46181237G>A , CM000681.1:g.46181237G>A	GRCh37
NC_000019.8:g.50873077G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.998G>A MANE Select	ENSP00000467494.1:p.Arg333Gln
ENST00000652180.1:c.815G>A	ENSP00000498426.1:p.Arg272Gln
ENST00000263281.7:c.998G>A	ENSP00000263281.3:p.Arg333Gln
ENST00000304207.12:c.890G>A	ENSP00000305321.8:p.Arg297Gln
ENST00000585889.1:c.*69G>A	ENSP00000467342.1:n.*69G>A
ENST00000590918.5:c.998G>A	ENSP00000467494.1:p.Arg333Gln
ENST00000591224.1:n.454G>A
ENST00000593127.1:n.99G>A
NM_000164.2:c.998G>A	NP_000155.1:p.Arg333Gln
NM_000164.3:c.998G>A	NP_000155.1:p.Arg333Gln
NM_001308418.1:c.890G>A	NP_001295347.1:p.Arg297Gln
XM_011526709.1:c.1124G>A	XP_011525011.1:p.Arg375Gln
XM_011526710.1:c.1124G>A	XP_011525012.1:p.Arg375Gln
XM_011526711.1:c.1016G>A	XP_011525013.1:p.Arg339Gln
XM_011526712.1:c.890G>A	XP_011525014.1:p.Arg297Gln
XM_011526713.1:c.875G>A	XP_011525015.1:p.Arg292Gln
XM_011526714.1:c.707G>A	XP_011525016.1:p.Arg236Gln
XM_011526715.1:c.707G>A	XP_011525017.1:p.Arg236Gln
XM_011526716.1:c.*82G>A	XP_011525018.1:n.*82G>A
XM_011526717.1:c.*82G>A	XP_011525019.1:n.*82G>A
XR_935791.1:n.1017G>A
XM_011526709.2:c.1124G>A	XP_011525011.1:p.Arg375Gln
XM_011526710.2:c.1124G>A	XP_011525012.1:p.Arg375Gln
XM_011526711.2:c.1016G>A	XP_011525013.1:p.Arg339Gln
XM_011526713.2:c.875G>A	XP_011525015.1:p.Arg292Gln
XM_011526714.2:c.707G>A	XP_011525016.1:p.Arg236Gln
XM_011526715.2:c.707G>A	XP_011525017.1:p.Arg236Gln
XM_011526716.2:c.*82G>A	XP_011525018.1:n.*82G>A
XM_017026584.1:c.653G>A	XP_016882073.1:p.Arg218Gln
XM_017026585.1:c.632G>A	XP_016882074.1:p.Arg211Gln
XM_017026586.1:c.509G>A	XP_016882075.1:p.Arg170Gln
XM_017026587.1:c.506G>A	XP_016882076.1:p.Arg169Gln
XR_001753655.1:n.1093G>A
XR_935791.2:n.1023G>A
NM_000164.4:c.998G>A MANE Select	NP_000155.1:p.Arg333Gln
NM_001308418.2:c.890G>A	NP_001295347.1:p.Arg297Gln