Canonical Allele Identifier: CA2338552561

Gene: GIPR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678857_45678858delinsAC , CM000681.2:g.45678857_45678858delinsAC	GRCh38
NC_000019.9:g.46182115_46182116delinsAC , CM000681.1:g.46182115_46182116delinsAC	GRCh37
NC_000019.8:g.50873955_50873956delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000590918.6:c.1152+631_1152+632delinsAC MANE Select	ENSP00000467494.1:n.1152+631_1152+632delinsAC
ENST00000652180.1:c.969+631_969+632delinsAC	ENSP00000498426.1:n.969+631_969+632delinsAC
ENST00000263281.7:c.1152+631_1152+632delinsAC	ENSP00000263281.3:n.1152+631_1152+632delinsAC
ENST00000304207.12:c.1044+631_1044+632delinsAC	ENSP00000305321.8:n.1044+631_1044+632delinsAC
ENST00000585889.1:c.*223+631_*223+632delinsAC	ENSP00000467342.1:n.*223+631_*223+632delinsAC
ENST00000590918.5:c.1152+631_1152+632delinsAC	ENSP00000467494.1:n.1152+631_1152+632delinsAC
NM_000164.2:c.1152+631_1152+632delinsAC	NP_000155.1:n.1152+631_1152+632delinsAC
NM_000164.3:c.1152+631_1152+632delinsAC	NP_000155.1:n.1152+631_1152+632delinsAC
NM_001308418.1:c.1044+631_1044+632delinsAC	NP_001295347.1:n.1044+631_1044+632delinsAC
XM_011526709.1:c.1278+631_1278+632delinsAC	XP_011525011.1:n.1278+631_1278+632delinsAC
XM_011526710.1:c.1278+631_1278+632delinsAC	XP_011525012.1:n.1278+631_1278+632delinsAC
XM_011526711.1:c.1170+631_1170+632delinsAC	XP_011525013.1:n.1170+631_1170+632delinsAC
XM_011526712.1:c.1044+631_1044+632delinsAC	XP_011525014.1:n.1044+631_1044+632delinsAC
XM_011526713.1:c.1029+631_1029+632delinsAC	XP_011525015.1:n.1029+631_1029+632delinsAC
XM_011526714.1:c.861+631_861+632delinsAC	XP_011525016.1:n.861+631_861+632delinsAC
XM_011526715.1:c.861+631_861+632delinsAC	XP_011525017.1:n.861+631_861+632delinsAC
XR_935791.1:n.1171+631_1171+632delinsAC
XM_011526709.2:c.1278+631_1278+632delinsAC	XP_011525011.1:n.1278+631_1278+632delinsAC
XM_011526710.2:c.1278+631_1278+632delinsAC	XP_011525012.1:n.1278+631_1278+632delinsAC
XM_011526711.2:c.1170+631_1170+632delinsAC	XP_011525013.1:n.1170+631_1170+632delinsAC
XM_011526713.2:c.1029+631_1029+632delinsAC	XP_011525015.1:n.1029+631_1029+632delinsAC
XM_011526714.2:c.861+631_861+632delinsAC	XP_011525016.1:n.861+631_861+632delinsAC
XM_011526715.2:c.861+631_861+632delinsAC	XP_011525017.1:n.861+631_861+632delinsAC
XM_017026584.1:c.807+631_807+632delinsAC	XP_016882073.1:n.807+631_807+632delinsAC
XM_017026585.1:c.786+631_786+632delinsAC	XP_016882074.1:n.786+631_786+632delinsAC
XM_017026586.1:c.663+631_663+632delinsAC	XP_016882075.1:n.663+631_663+632delinsAC
XM_017026587.1:c.660+631_660+632delinsAC	XP_016882076.1:n.660+631_660+632delinsAC
XR_001753655.1:n.1247+631_1247+632delinsAC
XR_935791.2:n.1177+631_1177+632delinsAC
NM_000164.4:c.1152+631_1152+632delinsAC MANE Select	NP_000155.1:n.1152+631_1152+632delinsAC
NM_001308418.2:c.1044+631_1044+632delinsAC	NP_001295347.1:n.1044+631_1044+632delinsAC