Canonical Allele Identifier: CA2338552120

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677938C= , CM000681.2:g.45677938C=	GRCh38
NC_000019.9:g.46181196C= , CM000681.1:g.46181196C=	GRCh37
NC_000019.8:g.50873036C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.957C= MANE Select	ENSP00000467494.1:p.Gly319=
ENST00000652180.1:c.774C=	ENSP00000498426.1:p.Gly258=
ENST00000263281.7:c.957C=	ENSP00000263281.3:p.Gly319=
ENST00000304207.12:c.849C=	ENSP00000305321.8:p.Gly283=
ENST00000585889.1:c.*28C=	ENSP00000467342.1:n.*28C=
ENST00000590918.5:c.957C=	ENSP00000467494.1:p.Gly319=
ENST00000591224.1:n.413C=
ENST00000593127.1:n.58C=
NM_000164.2:c.957C=	NP_000155.1:p.Gly319=
NM_000164.3:c.957C=	NP_000155.1:p.Gly319=
NM_001308418.1:c.849C=	NP_001295347.1:p.Gly283=
XM_011526709.1:c.1083C=	XP_011525011.1:p.Gly361=
XM_011526710.1:c.1083C=	XP_011525012.1:p.Gly361=
XM_011526711.1:c.975C=	XP_011525013.1:p.Gly325=
XM_011526712.1:c.849C=	XP_011525014.1:p.Gly283=
XM_011526713.1:c.834C=	XP_011525015.1:p.Gly278=
XM_011526714.1:c.666C=	XP_011525016.1:p.Gly222=
XM_011526715.1:c.666C=	XP_011525017.1:p.Gly222=
XM_011526716.1:c.*41C=	XP_011525018.1:n.*41C=
XM_011526717.1:c.*41C=	XP_011525019.1:n.*41C=
XR_935791.1:n.976C=
XM_011526709.2:c.1083C=	XP_011525011.1:p.Gly361=
XM_011526710.2:c.1083C=	XP_011525012.1:p.Gly361=
XM_011526711.2:c.975C=	XP_011525013.1:p.Gly325=
XM_011526713.2:c.834C=	XP_011525015.1:p.Gly278=
XM_011526714.2:c.666C=	XP_011525016.1:p.Gly222=
XM_011526715.2:c.666C=	XP_011525017.1:p.Gly222=
XM_011526716.2:c.*41C=	XP_011525018.1:n.*41C=
XM_017026584.1:c.612C=	XP_016882073.1:p.Gly204=
XM_017026585.1:c.591C=	XP_016882074.1:p.Gly197=
XM_017026586.1:c.468C=	XP_016882075.1:p.Gly156=
XM_017026587.1:c.465C=	XP_016882076.1:p.Gly155=
XR_001753655.1:n.1052C=
XR_935791.2:n.982C=
NM_000164.4:c.957C= MANE Select	NP_000155.1:p.Gly319=
NM_001308418.2:c.849C=	NP_001295347.1:p.Gly283=