Canonical Allele Identifier: CA2338552123

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677944C= , CM000681.2:g.45677944C=	GRCh38
NC_000019.9:g.46181202C= , CM000681.1:g.46181202C=	GRCh37
NC_000019.8:g.50873042C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.963C= MANE Select	ENSP00000467494.1:p.Leu321=
ENST00000652180.1:c.780C=	ENSP00000498426.1:p.Leu260=
ENST00000263281.7:c.963C=	ENSP00000263281.3:p.Leu321=
ENST00000304207.12:c.855C=	ENSP00000305321.8:p.Leu285=
ENST00000585889.1:c.*34C=	ENSP00000467342.1:n.*34C=
ENST00000590918.5:c.963C=	ENSP00000467494.1:p.Leu321=
ENST00000591224.1:n.419C=
ENST00000593127.1:n.64C=
NM_000164.2:c.963C=	NP_000155.1:p.Leu321=
NM_000164.3:c.963C=	NP_000155.1:p.Leu321=
NM_001308418.1:c.855C=	NP_001295347.1:p.Leu285=
XM_011526709.1:c.1089C=	XP_011525011.1:p.Leu363=
XM_011526710.1:c.1089C=	XP_011525012.1:p.Leu363=
XM_011526711.1:c.981C=	XP_011525013.1:p.Leu327=
XM_011526712.1:c.855C=	XP_011525014.1:p.Leu285=
XM_011526713.1:c.840C=	XP_011525015.1:p.Leu280=
XM_011526714.1:c.672C=	XP_011525016.1:p.Leu224=
XM_011526715.1:c.672C=	XP_011525017.1:p.Leu224=
XM_011526716.1:c.*47C=	XP_011525018.1:n.*47C=
XM_011526717.1:c.*47C=	XP_011525019.1:n.*47C=
XR_935791.1:n.982C=
XM_011526709.2:c.1089C=	XP_011525011.1:p.Leu363=
XM_011526710.2:c.1089C=	XP_011525012.1:p.Leu363=
XM_011526711.2:c.981C=	XP_011525013.1:p.Leu327=
XM_011526713.2:c.840C=	XP_011525015.1:p.Leu280=
XM_011526714.2:c.672C=	XP_011525016.1:p.Leu224=
XM_011526715.2:c.672C=	XP_011525017.1:p.Leu224=
XM_011526716.2:c.*47C=	XP_011525018.1:n.*47C=
XM_017026584.1:c.618C=	XP_016882073.1:p.Leu206=
XM_017026585.1:c.597C=	XP_016882074.1:p.Leu199=
XM_017026586.1:c.474C=	XP_016882075.1:p.Leu158=
XM_017026587.1:c.471C=	XP_016882076.1:p.Leu157=
XR_001753655.1:n.1058C=
XR_935791.2:n.988C=
NM_000164.4:c.963C= MANE Select	NP_000155.1:p.Leu321=
NM_001308418.2:c.855C=	NP_001295347.1:p.Leu285=