Canonical Allele Identifier: CA882740926

Gene: GIPR

Linked Data

• dbSNP Id: rs1165701720
• MyVariant Identifiers: chr19:g.46182255G>C (hg19) ; chr19:g.45678997G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678997G>C , CM000681.2:g.45678997G>C	GRCh38
NC_000019.9:g.46182255G>C , CM000681.1:g.46182255G>C	GRCh37
NC_000019.8:g.50874095G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1152+771G>C MANE Select	ENSP00000467494.1:n.1152+771G>C
ENST00000652180.1:c.969+771G>C	ENSP00000498426.1:n.969+771G>C
ENST00000263281.7:c.1152+771G>C	ENSP00000263281.3:n.1152+771G>C
ENST00000304207.12:c.1044+771G>C	ENSP00000305321.8:n.1044+771G>C
ENST00000585889.1:c.*223+771G>C	ENSP00000467342.1:n.*223+771G>C
ENST00000590918.5:c.1152+771G>C	ENSP00000467494.1:n.1152+771G>C
NM_000164.2:c.1152+771G>C	NP_000155.1:n.1152+771G>C
NM_000164.3:c.1152+771G>C	NP_000155.1:n.1152+771G>C
NM_001308418.1:c.1044+771G>C	NP_001295347.1:n.1044+771G>C
XM_011526709.1:c.1278+771G>C	XP_011525011.1:n.1278+771G>C
XM_011526710.1:c.1278+771G>C	XP_011525012.1:n.1278+771G>C
XM_011526711.1:c.1170+771G>C	XP_011525013.1:n.1170+771G>C
XM_011526712.1:c.1044+771G>C	XP_011525014.1:n.1044+771G>C
XM_011526713.1:c.1029+771G>C	XP_011525015.1:n.1029+771G>C
XM_011526714.1:c.861+771G>C	XP_011525016.1:n.861+771G>C
XM_011526715.1:c.861+771G>C	XP_011525017.1:n.861+771G>C
XR_935791.1:n.1171+771G>C
XM_011526709.2:c.1278+771G>C	XP_011525011.1:n.1278+771G>C
XM_011526710.2:c.1278+771G>C	XP_011525012.1:n.1278+771G>C
XM_011526711.2:c.1170+771G>C	XP_011525013.1:n.1170+771G>C
XM_011526713.2:c.1029+771G>C	XP_011525015.1:n.1029+771G>C
XM_011526714.2:c.861+771G>C	XP_011525016.1:n.861+771G>C
XM_011526715.2:c.861+771G>C	XP_011525017.1:n.861+771G>C
XM_017026584.1:c.807+771G>C	XP_016882073.1:n.807+771G>C
XM_017026585.1:c.786+771G>C	XP_016882074.1:n.786+771G>C
XM_017026586.1:c.663+771G>C	XP_016882075.1:n.663+771G>C
XM_017026587.1:c.660+771G>C	XP_016882076.1:n.660+771G>C
XR_001753655.1:n.1247+771G>C
XR_935791.2:n.1177+771G>C
NM_000164.4:c.1152+771G>C MANE Select	NP_000155.1:n.1152+771G>C
NM_001308418.2:c.1044+771G>C	NP_001295347.1:n.1044+771G>C