Canonical Allele Identifier: CA406395109

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181206T>A (hg19) ; chr19:g.45677948T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677948T>A , CM000681.2:g.45677948T>A	GRCh38
NC_000019.9:g.46181206T>A , CM000681.1:g.46181206T>A	GRCh37
NC_000019.8:g.50873046T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.967T>A MANE Select	ENSP00000467494.1:p.Ser323Thr
ENST00000652180.1:c.784T>A	ENSP00000498426.1:p.Ser262Thr
ENST00000263281.7:c.967T>A	ENSP00000263281.3:p.Ser323Thr
ENST00000304207.12:c.859T>A	ENSP00000305321.8:p.Ser287Thr
ENST00000585889.1:c.*38T>A	ENSP00000467342.1:n.*38T>A
ENST00000590918.5:c.967T>A	ENSP00000467494.1:p.Ser323Thr
ENST00000591224.1:n.423T>A
ENST00000593127.1:n.68T>A
NM_000164.2:c.967T>A	NP_000155.1:p.Ser323Thr
NM_000164.3:c.967T>A	NP_000155.1:p.Ser323Thr
NM_001308418.1:c.859T>A	NP_001295347.1:p.Ser287Thr
XM_011526709.1:c.1093T>A	XP_011525011.1:p.Ser365Thr
XM_011526710.1:c.1093T>A	XP_011525012.1:p.Ser365Thr
XM_011526711.1:c.985T>A	XP_011525013.1:p.Ser329Thr
XM_011526712.1:c.859T>A	XP_011525014.1:p.Ser287Thr
XM_011526713.1:c.844T>A	XP_011525015.1:p.Ser282Thr
XM_011526714.1:c.676T>A	XP_011525016.1:p.Ser226Thr
XM_011526715.1:c.676T>A	XP_011525017.1:p.Ser226Thr
XM_011526716.1:c.*51T>A	XP_011525018.1:n.*51T>A
XM_011526717.1:c.*51T>A	XP_011525019.1:n.*51T>A
XR_935791.1:n.986T>A
XM_011526709.2:c.1093T>A	XP_011525011.1:p.Ser365Thr
XM_011526710.2:c.1093T>A	XP_011525012.1:p.Ser365Thr
XM_011526711.2:c.985T>A	XP_011525013.1:p.Ser329Thr
XM_011526713.2:c.844T>A	XP_011525015.1:p.Ser282Thr
XM_011526714.2:c.676T>A	XP_011525016.1:p.Ser226Thr
XM_011526715.2:c.676T>A	XP_011525017.1:p.Ser226Thr
XM_011526716.2:c.*51T>A	XP_011525018.1:n.*51T>A
XM_017026584.1:c.622T>A	XP_016882073.1:p.Ser208Thr
XM_017026585.1:c.601T>A	XP_016882074.1:p.Ser201Thr
XM_017026586.1:c.478T>A	XP_016882075.1:p.Ser160Thr
XM_017026587.1:c.475T>A	XP_016882076.1:p.Ser159Thr
XR_001753655.1:n.1062T>A
XR_935791.2:n.992T>A
NM_000164.4:c.967T>A MANE Select	NP_000155.1:p.Ser323Thr
NM_001308418.2:c.859T>A	NP_001295347.1:p.Ser287Thr