Canonical Allele Identifier: CA406395529

Gene: GIPR

Linked Data

• dbSNP Id: rs1206338770
• gnomAD v4: 19-45678147-C-T
• MyVariant Identifiers: chr19:g.46181405C>T (hg19) ; chr19:g.45678147C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678147C>T , CM000681.2:g.45678147C>T	GRCh38
NC_000019.9:g.46181405C>T , CM000681.1:g.46181405C>T	GRCh37
NC_000019.8:g.50873245C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1073C>T MANE Select	ENSP00000467494.1:p.Ala358Val
ENST00000652180.1:c.890C>T	ENSP00000498426.1:p.Ala297Val
ENST00000263281.7:c.1073C>T	ENSP00000263281.3:p.Ala358Val
ENST00000304207.12:c.965C>T	ENSP00000305321.8:p.Ala322Val
ENST00000585889.1:c.*144C>T	ENSP00000467342.1:n.*144C>T
ENST00000590918.5:c.1073C>T	ENSP00000467494.1:p.Ala358Val
ENST00000591224.1:n.529C>T
NM_000164.2:c.1073C>T	NP_000155.1:p.Ala358Val
NM_000164.3:c.1073C>T	NP_000155.1:p.Ala358Val
NM_001308418.1:c.965C>T	NP_001295347.1:p.Ala322Val
XM_011526709.1:c.1199C>T	XP_011525011.1:p.Ala400Val
XM_011526710.1:c.1199C>T	XP_011525012.1:p.Ala400Val
XM_011526711.1:c.1091C>T	XP_011525013.1:p.Ala364Val
XM_011526712.1:c.965C>T	XP_011525014.1:p.Ala322Val
XM_011526713.1:c.950C>T	XP_011525015.1:p.Ala317Val
XM_011526714.1:c.782C>T	XP_011525016.1:p.Ala261Val
XM_011526715.1:c.782C>T	XP_011525017.1:p.Ala261Val
XR_935791.1:n.1092C>T
XM_011526709.2:c.1199C>T	XP_011525011.1:p.Ala400Val
XM_011526710.2:c.1199C>T	XP_011525012.1:p.Ala400Val
XM_011526711.2:c.1091C>T	XP_011525013.1:p.Ala364Val
XM_011526713.2:c.950C>T	XP_011525015.1:p.Ala317Val
XM_011526714.2:c.782C>T	XP_011525016.1:p.Ala261Val
XM_011526715.2:c.782C>T	XP_011525017.1:p.Ala261Val
XM_017026584.1:c.728C>T	XP_016882073.1:p.Ala243Val
XM_017026585.1:c.707C>T	XP_016882074.1:p.Ala236Val
XM_017026586.1:c.584C>T	XP_016882075.1:p.Ala195Val
XM_017026587.1:c.581C>T	XP_016882076.1:p.Ala194Val
XR_001753655.1:n.1168C>T
XR_935791.2:n.1098C>T
NM_000164.4:c.1073C>T MANE Select	NP_000155.1:p.Ala358Val
NM_001308418.2:c.965C>T	NP_001295347.1:p.Ala322Val