Canonical Allele Identifier: CA507825204

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181406T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678148T>A , CM000681.2:g.45678148T>A	GRCh38
NC_000019.9:g.46181406T>A , CM000681.1:g.46181406T>A	GRCh37
NC_000019.8:g.50873246T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1074T>A MANE Select	ENSP00000467494.1:p.Ala358=
ENST00000652180.1:c.891T>A	ENSP00000498426.1:p.Ala297=
ENST00000263281.7:c.1074T>A	ENSP00000263281.3:p.Ala358=
ENST00000304207.12:c.966T>A	ENSP00000305321.8:p.Ala322=
ENST00000585889.1:c.*145T>A	ENSP00000467342.1:n.*145T>A
ENST00000590918.5:c.1074T>A	ENSP00000467494.1:p.Ala358=
ENST00000591224.1:n.530T>A
NM_000164.2:c.1074T>A	NP_000155.1:p.Ala358=
NM_000164.3:c.1074T>A	NP_000155.1:p.Ala358=
NM_001308418.1:c.966T>A	NP_001295347.1:p.Ala322=
XM_011526709.1:c.1200T>A	XP_011525011.1:p.Ala400=
XM_011526710.1:c.1200T>A	XP_011525012.1:p.Ala400=
XM_011526711.1:c.1092T>A	XP_011525013.1:p.Ala364=
XM_011526712.1:c.966T>A	XP_011525014.1:p.Ala322=
XM_011526713.1:c.951T>A	XP_011525015.1:p.Ala317=
XM_011526714.1:c.783T>A	XP_011525016.1:p.Ala261=
XM_011526715.1:c.783T>A	XP_011525017.1:p.Ala261=
XR_935791.1:n.1093T>A
XM_011526709.2:c.1200T>A	XP_011525011.1:p.Ala400=
XM_011526710.2:c.1200T>A	XP_011525012.1:p.Ala400=
XM_011526711.2:c.1092T>A	XP_011525013.1:p.Ala364=
XM_011526713.2:c.951T>A	XP_011525015.1:p.Ala317=
XM_011526714.2:c.783T>A	XP_011525016.1:p.Ala261=
XM_011526715.2:c.783T>A	XP_011525017.1:p.Ala261=
XM_017026584.1:c.729T>A	XP_016882073.1:p.Ala243=
XM_017026585.1:c.708T>A	XP_016882074.1:p.Ala236=
XM_017026586.1:c.585T>A	XP_016882075.1:p.Ala195=
XM_017026587.1:c.582T>A	XP_016882076.1:p.Ala194=
XR_001753655.1:n.1169T>A
XR_935791.2:n.1099T>A
NM_000164.4:c.1074T>A MANE Select	NP_000155.1:p.Ala358=
NM_001308418.2:c.966T>A	NP_001295347.1:p.Ala322=