Canonical Allele Identifier: CA406395206

Gene: GIPR

Linked Data

• dbSNP Id: rs1467777931
• gnomAD v2: 19-46181233-T-C
• gnomAD v4: 19-45677975-T-C
• MyVariant Identifiers: chr19:g.46181233T>C (hg19) ; chr19:g.45677975T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677975T>C , CM000681.2:g.45677975T>C	GRCh38
NC_000019.9:g.46181233T>C , CM000681.1:g.46181233T>C	GRCh37
NC_000019.8:g.50873073T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.994T>C MANE Select	ENSP00000467494.1:p.Cys332Arg
ENST00000652180.1:c.811T>C	ENSP00000498426.1:p.Cys271Arg
ENST00000263281.7:c.994T>C	ENSP00000263281.3:p.Cys332Arg
ENST00000304207.12:c.886T>C	ENSP00000305321.8:p.Cys296Arg
ENST00000585889.1:c.*65T>C	ENSP00000467342.1:n.*65T>C
ENST00000590918.5:c.994T>C	ENSP00000467494.1:p.Cys332Arg
ENST00000591224.1:n.450T>C
ENST00000593127.1:n.95T>C
NM_000164.2:c.994T>C	NP_000155.1:p.Cys332Arg
NM_000164.3:c.994T>C	NP_000155.1:p.Cys332Arg
NM_001308418.1:c.886T>C	NP_001295347.1:p.Cys296Arg
XM_011526709.1:c.1120T>C	XP_011525011.1:p.Cys374Arg
XM_011526710.1:c.1120T>C	XP_011525012.1:p.Cys374Arg
XM_011526711.1:c.1012T>C	XP_011525013.1:p.Cys338Arg
XM_011526712.1:c.886T>C	XP_011525014.1:p.Cys296Arg
XM_011526713.1:c.871T>C	XP_011525015.1:p.Cys291Arg
XM_011526714.1:c.703T>C	XP_011525016.1:p.Cys235Arg
XM_011526715.1:c.703T>C	XP_011525017.1:p.Cys235Arg
XM_011526716.1:c.*78T>C	XP_011525018.1:n.*78T>C
XM_011526717.1:c.*78T>C	XP_011525019.1:n.*78T>C
XR_935791.1:n.1013T>C
XM_011526709.2:c.1120T>C	XP_011525011.1:p.Cys374Arg
XM_011526710.2:c.1120T>C	XP_011525012.1:p.Cys374Arg
XM_011526711.2:c.1012T>C	XP_011525013.1:p.Cys338Arg
XM_011526713.2:c.871T>C	XP_011525015.1:p.Cys291Arg
XM_011526714.2:c.703T>C	XP_011525016.1:p.Cys235Arg
XM_011526715.2:c.703T>C	XP_011525017.1:p.Cys235Arg
XM_011526716.2:c.*78T>C	XP_011525018.1:n.*78T>C
XM_017026584.1:c.649T>C	XP_016882073.1:p.Cys217Arg
XM_017026585.1:c.628T>C	XP_016882074.1:p.Cys210Arg
XM_017026586.1:c.505T>C	XP_016882075.1:p.Cys169Arg
XM_017026587.1:c.502T>C	XP_016882076.1:p.Cys168Arg
XR_001753655.1:n.1089T>C
XR_935791.2:n.1019T>C
NM_000164.4:c.994T>C MANE Select	NP_000155.1:p.Cys332Arg
NM_001308418.2:c.886T>C	NP_001295347.1:p.Cys296Arg