Canonical Allele Identifier: CA406395547

Gene: GIPR

Linked Data

• dbSNP Id: rs1213210232
• gnomAD v2: 19-46181411-T-C
• gnomAD v4: 19-45678153-T-C
• MyVariant Identifiers: chr19:g.46181411T>C (hg19) ; chr19:g.45678153T>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000590918.6:c.1079T>C MANE Select	ENSP00000467494.1:p.Val360Ala
ENST00000652180.1:c.896T>C	ENSP00000498426.1:p.Val299Ala
ENST00000263281.7:c.1079T>C	ENSP00000263281.3:p.Val360Ala
ENST00000304207.12:c.971T>C	ENSP00000305321.8:p.Val324Ala
ENST00000585889.1:c.*150T>C	ENSP00000467342.1:n.*150T>C
ENST00000590918.5:c.1079T>C	ENSP00000467494.1:p.Val360Ala
ENST00000591224.1:n.535T>C
NM_000164.2:c.1079T>C	NP_000155.1:p.Val360Ala
NM_000164.3:c.1079T>C	NP_000155.1:p.Val360Ala
NM_001308418.1:c.971T>C	NP_001295347.1:p.Val324Ala
XM_011526709.1:c.1205T>C	XP_011525011.1:p.Val402Ala
XM_011526710.1:c.1205T>C	XP_011525012.1:p.Val402Ala
XM_011526711.1:c.1097T>C	XP_011525013.1:p.Val366Ala
XM_011526712.1:c.971T>C	XP_011525014.1:p.Val324Ala
XM_011526713.1:c.956T>C	XP_011525015.1:p.Val319Ala
XM_011526714.1:c.788T>C	XP_011525016.1:p.Val263Ala
XM_011526715.1:c.788T>C	XP_011525017.1:p.Val263Ala
XR_935791.1:n.1098T>C
XM_011526709.2:c.1205T>C	XP_011525011.1:p.Val402Ala
XM_011526710.2:c.1205T>C	XP_011525012.1:p.Val402Ala
XM_011526711.2:c.1097T>C	XP_011525013.1:p.Val366Ala
XM_011526713.2:c.956T>C	XP_011525015.1:p.Val319Ala
XM_011526714.2:c.788T>C	XP_011525016.1:p.Val263Ala
XM_011526715.2:c.788T>C	XP_011525017.1:p.Val263Ala
XM_017026584.1:c.734T>C	XP_016882073.1:p.Val245Ala
XM_017026585.1:c.713T>C	XP_016882074.1:p.Val238Ala
XM_017026586.1:c.590T>C	XP_016882075.1:p.Val197Ala
XM_017026587.1:c.587T>C	XP_016882076.1:p.Val196Ala
XR_001753655.1:n.1174T>C
XR_935791.2:n.1104T>C
NM_000164.4:c.1079T>C MANE Select	NP_000155.1:p.Val360Ala
NM_001308418.2:c.971T>C	NP_001295347.1:p.Val324Ala