Canonical Allele Identifier: CA406395156

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181219C>A (hg19) ; chr19:g.45677961C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677961C>A , CM000681.2:g.45677961C>A	GRCh38
NC_000019.9:g.46181219C>A , CM000681.1:g.46181219C>A	GRCh37
NC_000019.8:g.50873059C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.980C>A MANE Select	ENSP00000467494.1:p.Thr327Lys
ENST00000652180.1:c.797C>A	ENSP00000498426.1:p.Thr266Lys
ENST00000263281.7:c.980C>A	ENSP00000263281.3:p.Thr327Lys
ENST00000304207.12:c.872C>A	ENSP00000305321.8:p.Thr291Lys
ENST00000585889.1:c.*51C>A	ENSP00000467342.1:n.*51C>A
ENST00000590918.5:c.980C>A	ENSP00000467494.1:p.Thr327Lys
ENST00000591224.1:n.436C>A
ENST00000593127.1:n.81C>A
NM_000164.2:c.980C>A	NP_000155.1:p.Thr327Lys
NM_000164.3:c.980C>A	NP_000155.1:p.Thr327Lys
NM_001308418.1:c.872C>A	NP_001295347.1:p.Thr291Lys
XM_011526709.1:c.1106C>A	XP_011525011.1:p.Thr369Lys
XM_011526710.1:c.1106C>A	XP_011525012.1:p.Thr369Lys
XM_011526711.1:c.998C>A	XP_011525013.1:p.Thr333Lys
XM_011526712.1:c.872C>A	XP_011525014.1:p.Thr291Lys
XM_011526713.1:c.857C>A	XP_011525015.1:p.Thr286Lys
XM_011526714.1:c.689C>A	XP_011525016.1:p.Thr230Lys
XM_011526715.1:c.689C>A	XP_011525017.1:p.Thr230Lys
XM_011526716.1:c.*64C>A	XP_011525018.1:n.*64C>A
XM_011526717.1:c.*64C>A	XP_011525019.1:n.*64C>A
XR_935791.1:n.999C>A
XM_011526709.2:c.1106C>A	XP_011525011.1:p.Thr369Lys
XM_011526710.2:c.1106C>A	XP_011525012.1:p.Thr369Lys
XM_011526711.2:c.998C>A	XP_011525013.1:p.Thr333Lys
XM_011526713.2:c.857C>A	XP_011525015.1:p.Thr286Lys
XM_011526714.2:c.689C>A	XP_011525016.1:p.Thr230Lys
XM_011526715.2:c.689C>A	XP_011525017.1:p.Thr230Lys
XM_011526716.2:c.*64C>A	XP_011525018.1:n.*64C>A
XM_017026584.1:c.635C>A	XP_016882073.1:p.Thr212Lys
XM_017026585.1:c.614C>A	XP_016882074.1:p.Thr205Lys
XM_017026586.1:c.491C>A	XP_016882075.1:p.Thr164Lys
XM_017026587.1:c.488C>A	XP_016882076.1:p.Thr163Lys
XR_001753655.1:n.1075C>A
XR_935791.2:n.1005C>A
NM_000164.4:c.980C>A MANE Select	NP_000155.1:p.Thr327Lys
NM_001308418.2:c.872C>A	NP_001295347.1:p.Thr291Lys