Canonical Allele Identifier: CA2338552225

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678152G= , CM000681.2:g.45678152G=	GRCh38
NC_000019.9:g.46181410G= , CM000681.1:g.46181410G=	GRCh37
NC_000019.8:g.50873250G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000590918.6:c.1078G= MANE Select	ENSP00000467494.1:p.Val360=
ENST00000652180.1:c.895G=	ENSP00000498426.1:p.Val299=
ENST00000263281.7:c.1078G=	ENSP00000263281.3:p.Val360=
ENST00000304207.12:c.970G=	ENSP00000305321.8:p.Val324=
ENST00000585889.1:c.*149G=	ENSP00000467342.1:n.*149G=
ENST00000590918.5:c.1078G=	ENSP00000467494.1:p.Val360=
ENST00000591224.1:n.534G=
NM_000164.2:c.1078G=	NP_000155.1:p.Val360=
NM_000164.3:c.1078G=	NP_000155.1:p.Val360=
NM_001308418.1:c.970G=	NP_001295347.1:p.Val324=
XM_011526709.1:c.1204G=	XP_011525011.1:p.Val402=
XM_011526710.1:c.1204G=	XP_011525012.1:p.Val402=
XM_011526711.1:c.1096G=	XP_011525013.1:p.Val366=
XM_011526712.1:c.970G=	XP_011525014.1:p.Val324=
XM_011526713.1:c.955G=	XP_011525015.1:p.Val319=
XM_011526714.1:c.787G=	XP_011525016.1:p.Val263=
XM_011526715.1:c.787G=	XP_011525017.1:p.Val263=
XR_935791.1:n.1097G=
XM_011526709.2:c.1204G=	XP_011525011.1:p.Val402=
XM_011526710.2:c.1204G=	XP_011525012.1:p.Val402=
XM_011526711.2:c.1096G=	XP_011525013.1:p.Val366=
XM_011526713.2:c.955G=	XP_011525015.1:p.Val319=
XM_011526714.2:c.787G=	XP_011525016.1:p.Val263=
XM_011526715.2:c.787G=	XP_011525017.1:p.Val263=
XM_017026584.1:c.733G=	XP_016882073.1:p.Val245=
XM_017026585.1:c.712G=	XP_016882074.1:p.Val238=
XM_017026586.1:c.589G=	XP_016882075.1:p.Val197=
XM_017026587.1:c.586G=	XP_016882076.1:p.Val196=
XR_001753655.1:n.1173G=
XR_935791.2:n.1103G=
NM_000164.4:c.1078G= MANE Select	NP_000155.1:p.Val360=
NM_001308418.2:c.970G=	NP_001295347.1:p.Val324=