Canonical Allele Identifier: CA920119389

Gene: GIPR

Linked Data

• dbSNP Id: rs1568526158

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677981del , CM000681.2:g.45677981del	GRCh38
NC_000019.9:g.46181239del , CM000681.1:g.46181239del	GRCh37
NC_000019.8:g.50873079del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1000del MANE Select	ENSP00000467494.1:p.Asp334IlefsTer4
ENST00000652180.1:c.817del	ENSP00000498426.1:p.Asp273IlefsTer4
ENST00000263281.7:c.1000del	ENSP00000263281.3:p.Asp334IlefsTer4
ENST00000304207.12:c.892del	ENSP00000305321.8:p.Asp298IlefsTer4
ENST00000585889.1:c.*71del	ENSP00000467342.1:n.*71del
ENST00000590918.5:c.1000del	ENSP00000467494.1:p.Asp334IlefsTer4
ENST00000591224.1:n.456del
ENST00000593127.1:n.101del
NM_000164.2:c.1000del	NP_000155.1:p.Asp334IlefsTer4
NM_000164.3:c.1000del	NP_000155.1:p.Asp334IlefsTer4
NM_001308418.1:c.892del	NP_001295347.1:p.Asp298IlefsTer4
XM_011526709.1:c.1126del	XP_011525011.1:p.Asp376IlefsTer4
XM_011526710.1:c.1126del	XP_011525012.1:p.Asp376IlefsTer4
XM_011526711.1:c.1018del	XP_011525013.1:p.Asp340IlefsTer4
XM_011526712.1:c.892del	XP_011525014.1:p.Asp298IlefsTer4
XM_011526713.1:c.877del	XP_011525015.1:p.Asp293IlefsTer4
XM_011526714.1:c.709del	XP_011525016.1:p.Asp237IlefsTer4
XM_011526715.1:c.709del	XP_011525017.1:p.Asp237IlefsTer4
XM_011526716.1:c.*84del	XP_011525018.1:n.*84del
XM_011526717.1:c.*84del	XP_011525019.1:n.*84del
XR_935791.1:n.1019del
XM_011526709.2:c.1126del	XP_011525011.1:p.Asp376IlefsTer4
XM_011526710.2:c.1126del	XP_011525012.1:p.Asp376IlefsTer4
XM_011526711.2:c.1018del	XP_011525013.1:p.Asp340IlefsTer4
XM_011526713.2:c.877del	XP_011525015.1:p.Asp293IlefsTer4
XM_011526714.2:c.709del	XP_011525016.1:p.Asp237IlefsTer4
XM_011526715.2:c.709del	XP_011525017.1:p.Asp237IlefsTer4
XM_011526716.2:c.*84del	XP_011525018.1:n.*84del
XM_017026584.1:c.655del	XP_016882073.1:p.Asp219IlefsTer4
XM_017026585.1:c.634del	XP_016882074.1:p.Asp212IlefsTer4
XM_017026586.1:c.511del	XP_016882075.1:p.Asp171IlefsTer4
XM_017026587.1:c.508del	XP_016882076.1:p.Asp170IlefsTer4
XR_001753655.1:n.1095del
XR_935791.2:n.1025del
NM_000164.4:c.1000del MANE Select	NP_000155.1:p.Asp334IlefsTer4
NM_001308418.2:c.892del	NP_001295347.1:p.Asp298IlefsTer4