Canonical Allele Identifier: CA2338552560

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678853C= , CM000681.2:g.45678853C=	GRCh38
NC_000019.9:g.46182111C= , CM000681.1:g.46182111C=	GRCh37
NC_000019.8:g.50873951C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1152+627C= MANE Select	ENSP00000467494.1:n.1152+627C=
ENST00000652180.1:c.969+627C=	ENSP00000498426.1:n.969+627C=
ENST00000263281.7:c.1152+627C=	ENSP00000263281.3:n.1152+627C=
ENST00000304207.12:c.1044+627C=	ENSP00000305321.8:n.1044+627C=
ENST00000585889.1:c.*223+627C=	ENSP00000467342.1:n.*223+627C=
ENST00000590918.5:c.1152+627C=	ENSP00000467494.1:n.1152+627C=
NM_000164.2:c.1152+627C=	NP_000155.1:n.1152+627C=
NM_000164.3:c.1152+627C=	NP_000155.1:n.1152+627C=
NM_001308418.1:c.1044+627C=	NP_001295347.1:n.1044+627C=
XM_011526709.1:c.1278+627C=	XP_011525011.1:n.1278+627C=
XM_011526710.1:c.1278+627C=	XP_011525012.1:n.1278+627C=
XM_011526711.1:c.1170+627C=	XP_011525013.1:n.1170+627C=
XM_011526712.1:c.1044+627C=	XP_011525014.1:n.1044+627C=
XM_011526713.1:c.1029+627C=	XP_011525015.1:n.1029+627C=
XM_011526714.1:c.861+627C=	XP_011525016.1:n.861+627C=
XM_011526715.1:c.861+627C=	XP_011525017.1:n.861+627C=
XR_935791.1:n.1171+627C=
XM_011526709.2:c.1278+627C=	XP_011525011.1:n.1278+627C=
XM_011526710.2:c.1278+627C=	XP_011525012.1:n.1278+627C=
XM_011526711.2:c.1170+627C=	XP_011525013.1:n.1170+627C=
XM_011526713.2:c.1029+627C=	XP_011525015.1:n.1029+627C=
XM_011526714.2:c.861+627C=	XP_011525016.1:n.861+627C=
XM_011526715.2:c.861+627C=	XP_011525017.1:n.861+627C=
XM_017026584.1:c.807+627C=	XP_016882073.1:n.807+627C=
XM_017026585.1:c.786+627C=	XP_016882074.1:n.786+627C=
XM_017026586.1:c.663+627C=	XP_016882075.1:n.663+627C=
XM_017026587.1:c.660+627C=	XP_016882076.1:n.660+627C=
XR_001753655.1:n.1247+627C=
XR_935791.2:n.1177+627C=
NM_000164.4:c.1152+627C= MANE Select	NP_000155.1:n.1152+627C=
NM_001308418.2:c.1044+627C=	NP_001295347.1:n.1044+627C=