Canonical Allele Identifier: CA406395079

Gene: GIPR

Linked Data

• COSMIC: COSM4573070 ; COSM4573071
• MyVariant Identifiers: chr19:g.46181198T>A (hg19) ; chr19:g.45677940T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677940T>A , CM000681.2:g.45677940T>A	GRCh38
NC_000019.9:g.46181198T>A , CM000681.1:g.46181198T>A	GRCh37
NC_000019.8:g.50873038T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.959T>A MANE Select	ENSP00000467494.1:p.Ile320Asn
ENST00000652180.1:c.776T>A	ENSP00000498426.1:p.Ile259Asn
ENST00000263281.7:c.959T>A	ENSP00000263281.3:p.Ile320Asn
ENST00000304207.12:c.851T>A	ENSP00000305321.8:p.Ile284Asn
ENST00000585889.1:c.*30T>A	ENSP00000467342.1:n.*30T>A
ENST00000590918.5:c.959T>A	ENSP00000467494.1:p.Ile320Asn
ENST00000591224.1:n.415T>A
ENST00000593127.1:n.60T>A
NM_000164.2:c.959T>A	NP_000155.1:p.Ile320Asn
NM_000164.3:c.959T>A	NP_000155.1:p.Ile320Asn
NM_001308418.1:c.851T>A	NP_001295347.1:p.Ile284Asn
XM_011526709.1:c.1085T>A	XP_011525011.1:p.Ile362Asn
XM_011526710.1:c.1085T>A	XP_011525012.1:p.Ile362Asn
XM_011526711.1:c.977T>A	XP_011525013.1:p.Ile326Asn
XM_011526712.1:c.851T>A	XP_011525014.1:p.Ile284Asn
XM_011526713.1:c.836T>A	XP_011525015.1:p.Ile279Asn
XM_011526714.1:c.668T>A	XP_011525016.1:p.Ile223Asn
XM_011526715.1:c.668T>A	XP_011525017.1:p.Ile223Asn
XM_011526716.1:c.*43T>A	XP_011525018.1:n.*43T>A
XM_011526717.1:c.*43T>A	XP_011525019.1:n.*43T>A
XR_935791.1:n.978T>A
XM_011526709.2:c.1085T>A	XP_011525011.1:p.Ile362Asn
XM_011526710.2:c.1085T>A	XP_011525012.1:p.Ile362Asn
XM_011526711.2:c.977T>A	XP_011525013.1:p.Ile326Asn
XM_011526713.2:c.836T>A	XP_011525015.1:p.Ile279Asn
XM_011526714.2:c.668T>A	XP_011525016.1:p.Ile223Asn
XM_011526715.2:c.668T>A	XP_011525017.1:p.Ile223Asn
XM_011526716.2:c.*43T>A	XP_011525018.1:n.*43T>A
XM_017026584.1:c.614T>A	XP_016882073.1:p.Ile205Asn
XM_017026585.1:c.593T>A	XP_016882074.1:p.Ile198Asn
XM_017026586.1:c.470T>A	XP_016882075.1:p.Ile157Asn
XM_017026587.1:c.467T>A	XP_016882076.1:p.Ile156Asn
XR_001753655.1:n.1054T>A
XR_935791.2:n.984T>A
NM_000164.4:c.959T>A MANE Select	NP_000155.1:p.Ile320Asn
NM_001308418.2:c.851T>A	NP_001295347.1:p.Ile284Asn