Canonical Allele Identifier: CA2338552119

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677937G= , CM000681.2:g.45677937G=	GRCh38
NC_000019.9:g.46181195G= , CM000681.1:g.46181195G=	GRCh37
NC_000019.8:g.50873035G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.956G= MANE Select	ENSP00000467494.1:p.Gly319=
ENST00000652180.1:c.773G=	ENSP00000498426.1:p.Gly258=
ENST00000263281.7:c.956G=	ENSP00000263281.3:p.Gly319=
ENST00000304207.12:c.848G=	ENSP00000305321.8:p.Gly283=
ENST00000585889.1:c.*27G=	ENSP00000467342.1:n.*27G=
ENST00000590918.5:c.956G=	ENSP00000467494.1:p.Gly319=
ENST00000591224.1:n.412G=
ENST00000593127.1:n.57G=
NM_000164.2:c.956G=	NP_000155.1:p.Gly319=
NM_000164.3:c.956G=	NP_000155.1:p.Gly319=
NM_001308418.1:c.848G=	NP_001295347.1:p.Gly283=
XM_011526709.1:c.1082G=	XP_011525011.1:p.Gly361=
XM_011526710.1:c.1082G=	XP_011525012.1:p.Gly361=
XM_011526711.1:c.974G=	XP_011525013.1:p.Gly325=
XM_011526712.1:c.848G=	XP_011525014.1:p.Gly283=
XM_011526713.1:c.833G=	XP_011525015.1:p.Gly278=
XM_011526714.1:c.665G=	XP_011525016.1:p.Gly222=
XM_011526715.1:c.665G=	XP_011525017.1:p.Gly222=
XM_011526716.1:c.*40G=	XP_011525018.1:n.*40G=
XM_011526717.1:c.*40G=	XP_011525019.1:n.*40G=
XR_935791.1:n.975G=
XM_011526709.2:c.1082G=	XP_011525011.1:p.Gly361=
XM_011526710.2:c.1082G=	XP_011525012.1:p.Gly361=
XM_011526711.2:c.974G=	XP_011525013.1:p.Gly325=
XM_011526713.2:c.833G=	XP_011525015.1:p.Gly278=
XM_011526714.2:c.665G=	XP_011525016.1:p.Gly222=
XM_011526715.2:c.665G=	XP_011525017.1:p.Gly222=
XM_011526716.2:c.*40G=	XP_011525018.1:n.*40G=
XM_017026584.1:c.611G=	XP_016882073.1:p.Gly204=
XM_017026585.1:c.590G=	XP_016882074.1:p.Gly197=
XM_017026586.1:c.467G=	XP_016882075.1:p.Gly156=
XM_017026587.1:c.464G=	XP_016882076.1:p.Gly155=
XR_001753655.1:n.1051G=
XR_935791.2:n.981G=
NM_000164.4:c.956G= MANE Select	NP_000155.1:p.Gly319=
NM_001308418.2:c.848G=	NP_001295347.1:p.Gly283=