Canonical Allele Identifier: CA882740921

Gene: GIPR

Linked Data

• dbSNP Id: rs1443533000
• gnomAD v3: 19-45678967-G-A
• gnomAD v4: 19-45678967-G-A
• MyVariant Identifiers: chr19:g.46182225G>A (hg19) ; chr19:g.45678967G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678967G>A , CM000681.2:g.45678967G>A	GRCh38
NC_000019.9:g.46182225G>A , CM000681.1:g.46182225G>A	GRCh37
NC_000019.8:g.50874065G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1152+741G>A MANE Select	ENSP00000467494.1:n.1152+741G>A
ENST00000652180.1:c.969+741G>A	ENSP00000498426.1:n.969+741G>A
ENST00000263281.7:c.1152+741G>A	ENSP00000263281.3:n.1152+741G>A
ENST00000304207.12:c.1044+741G>A	ENSP00000305321.8:n.1044+741G>A
ENST00000585889.1:c.*223+741G>A	ENSP00000467342.1:n.*223+741G>A
ENST00000590918.5:c.1152+741G>A	ENSP00000467494.1:n.1152+741G>A
NM_000164.2:c.1152+741G>A	NP_000155.1:n.1152+741G>A
NM_000164.3:c.1152+741G>A	NP_000155.1:n.1152+741G>A
NM_001308418.1:c.1044+741G>A	NP_001295347.1:n.1044+741G>A
XM_011526709.1:c.1278+741G>A	XP_011525011.1:n.1278+741G>A
XM_011526710.1:c.1278+741G>A	XP_011525012.1:n.1278+741G>A
XM_011526711.1:c.1170+741G>A	XP_011525013.1:n.1170+741G>A
XM_011526712.1:c.1044+741G>A	XP_011525014.1:n.1044+741G>A
XM_011526713.1:c.1029+741G>A	XP_011525015.1:n.1029+741G>A
XM_011526714.1:c.861+741G>A	XP_011525016.1:n.861+741G>A
XM_011526715.1:c.861+741G>A	XP_011525017.1:n.861+741G>A
XR_935791.1:n.1171+741G>A
XM_011526709.2:c.1278+741G>A	XP_011525011.1:n.1278+741G>A
XM_011526710.2:c.1278+741G>A	XP_011525012.1:n.1278+741G>A
XM_011526711.2:c.1170+741G>A	XP_011525013.1:n.1170+741G>A
XM_011526713.2:c.1029+741G>A	XP_011525015.1:n.1029+741G>A
XM_011526714.2:c.861+741G>A	XP_011525016.1:n.861+741G>A
XM_011526715.2:c.861+741G>A	XP_011525017.1:n.861+741G>A
XM_017026584.1:c.807+741G>A	XP_016882073.1:n.807+741G>A
XM_017026585.1:c.786+741G>A	XP_016882074.1:n.786+741G>A
XM_017026586.1:c.663+741G>A	XP_016882075.1:n.663+741G>A
XM_017026587.1:c.660+741G>A	XP_016882076.1:n.660+741G>A
XR_001753655.1:n.1247+741G>A
XR_935791.2:n.1177+741G>A
NM_000164.4:c.1152+741G>A MANE Select	NP_000155.1:n.1152+741G>A
NM_001308418.2:c.1044+741G>A	NP_001295347.1:n.1044+741G>A