Canonical Allele Identifier: CA406395177

Gene: GIPR

Linked Data

• gnomAD v4: 19-45677967-A-G
• MyVariant Identifiers: chr19:g.46181225A>G (hg19) ; chr19:g.45677967A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677967A>G , CM000681.2:g.45677967A>G	GRCh38
NC_000019.9:g.46181225A>G , CM000681.1:g.46181225A>G	GRCh37
NC_000019.8:g.50873065A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.986A>G MANE Select	ENSP00000467494.1:p.Gln329Arg
ENST00000652180.1:c.803A>G	ENSP00000498426.1:p.Gln268Arg
ENST00000263281.7:c.986A>G	ENSP00000263281.3:p.Gln329Arg
ENST00000304207.12:c.878A>G	ENSP00000305321.8:p.Gln293Arg
ENST00000585889.1:c.*57A>G	ENSP00000467342.1:n.*57A>G
ENST00000590918.5:c.986A>G	ENSP00000467494.1:p.Gln329Arg
ENST00000591224.1:n.442A>G
ENST00000593127.1:n.87A>G
NM_000164.2:c.986A>G	NP_000155.1:p.Gln329Arg
NM_000164.3:c.986A>G	NP_000155.1:p.Gln329Arg
NM_001308418.1:c.878A>G	NP_001295347.1:p.Gln293Arg
XM_011526709.1:c.1112A>G	XP_011525011.1:p.Gln371Arg
XM_011526710.1:c.1112A>G	XP_011525012.1:p.Gln371Arg
XM_011526711.1:c.1004A>G	XP_011525013.1:p.Gln335Arg
XM_011526712.1:c.878A>G	XP_011525014.1:p.Gln293Arg
XM_011526713.1:c.863A>G	XP_011525015.1:p.Gln288Arg
XM_011526714.1:c.695A>G	XP_011525016.1:p.Gln232Arg
XM_011526715.1:c.695A>G	XP_011525017.1:p.Gln232Arg
XM_011526716.1:c.*70A>G	XP_011525018.1:n.*70A>G
XM_011526717.1:c.*70A>G	XP_011525019.1:n.*70A>G
XR_935791.1:n.1005A>G
XM_011526709.2:c.1112A>G	XP_011525011.1:p.Gln371Arg
XM_011526710.2:c.1112A>G	XP_011525012.1:p.Gln371Arg
XM_011526711.2:c.1004A>G	XP_011525013.1:p.Gln335Arg
XM_011526713.2:c.863A>G	XP_011525015.1:p.Gln288Arg
XM_011526714.2:c.695A>G	XP_011525016.1:p.Gln232Arg
XM_011526715.2:c.695A>G	XP_011525017.1:p.Gln232Arg
XM_011526716.2:c.*70A>G	XP_011525018.1:n.*70A>G
XM_017026584.1:c.641A>G	XP_016882073.1:p.Gln214Arg
XM_017026585.1:c.620A>G	XP_016882074.1:p.Gln207Arg
XM_017026586.1:c.497A>G	XP_016882075.1:p.Gln166Arg
XM_017026587.1:c.494A>G	XP_016882076.1:p.Gln165Arg
XR_001753655.1:n.1081A>G
XR_935791.2:n.1011A>G
NM_000164.4:c.986A>G MANE Select	NP_000155.1:p.Gln329Arg
NM_001308418.2:c.878A>G	NP_001295347.1:p.Gln293Arg