Canonical Allele Identifier: CA406395544

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181411T>A (hg19) ; chr19:g.45678153T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678153T>A , CM000681.2:g.45678153T>A	GRCh38
NC_000019.9:g.46181411T>A , CM000681.1:g.46181411T>A	GRCh37
NC_000019.8:g.50873251T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1079T>A MANE Select	ENSP00000467494.1:p.Val360Glu
ENST00000652180.1:c.896T>A	ENSP00000498426.1:p.Val299Glu
ENST00000263281.7:c.1079T>A	ENSP00000263281.3:p.Val360Glu
ENST00000304207.12:c.971T>A	ENSP00000305321.8:p.Val324Glu
ENST00000585889.1:c.*150T>A	ENSP00000467342.1:n.*150T>A
ENST00000590918.5:c.1079T>A	ENSP00000467494.1:p.Val360Glu
ENST00000591224.1:n.535T>A
NM_000164.2:c.1079T>A	NP_000155.1:p.Val360Glu
NM_000164.3:c.1079T>A	NP_000155.1:p.Val360Glu
NM_001308418.1:c.971T>A	NP_001295347.1:p.Val324Glu
XM_011526709.1:c.1205T>A	XP_011525011.1:p.Val402Glu
XM_011526710.1:c.1205T>A	XP_011525012.1:p.Val402Glu
XM_011526711.1:c.1097T>A	XP_011525013.1:p.Val366Glu
XM_011526712.1:c.971T>A	XP_011525014.1:p.Val324Glu
XM_011526713.1:c.956T>A	XP_011525015.1:p.Val319Glu
XM_011526714.1:c.788T>A	XP_011525016.1:p.Val263Glu
XM_011526715.1:c.788T>A	XP_011525017.1:p.Val263Glu
XR_935791.1:n.1098T>A
XM_011526709.2:c.1205T>A	XP_011525011.1:p.Val402Glu
XM_011526710.2:c.1205T>A	XP_011525012.1:p.Val402Glu
XM_011526711.2:c.1097T>A	XP_011525013.1:p.Val366Glu
XM_011526713.2:c.956T>A	XP_011525015.1:p.Val319Glu
XM_011526714.2:c.788T>A	XP_011525016.1:p.Val263Glu
XM_011526715.2:c.788T>A	XP_011525017.1:p.Val263Glu
XM_017026584.1:c.734T>A	XP_016882073.1:p.Val245Glu
XM_017026585.1:c.713T>A	XP_016882074.1:p.Val238Glu
XM_017026586.1:c.590T>A	XP_016882075.1:p.Val197Glu
XM_017026587.1:c.587T>A	XP_016882076.1:p.Val196Glu
XR_001753655.1:n.1174T>A
XR_935791.2:n.1104T>A
NM_000164.4:c.1079T>A MANE Select	NP_000155.1:p.Val360Glu
NM_001308418.2:c.971T>A	NP_001295347.1:p.Val324Glu