Canonical Allele Identifier: CA507825128

Gene: GIPR

Linked Data

• dbSNP Id: rs1405568033
• gnomAD v2: 19-46181226-A-G
• gnomAD v4: 19-45677968-A-G
• MyVariant Identifiers: chr19:g.46181226A>G (hg19) ; chr19:g.45677968A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677968A>G , CM000681.2:g.45677968A>G	GRCh38
NC_000019.9:g.46181226A>G , CM000681.1:g.46181226A>G	GRCh37
NC_000019.8:g.50873066A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.987A>G MANE Select	ENSP00000467494.1:p.Gln329=
ENST00000652180.1:c.804A>G	ENSP00000498426.1:p.Gln268=
ENST00000263281.7:c.987A>G	ENSP00000263281.3:p.Gln329=
ENST00000304207.12:c.879A>G	ENSP00000305321.8:p.Gln293=
ENST00000585889.1:c.*58A>G	ENSP00000467342.1:n.*58A>G
ENST00000590918.5:c.987A>G	ENSP00000467494.1:p.Gln329=
ENST00000591224.1:n.443A>G
ENST00000593127.1:n.88A>G
NM_000164.2:c.987A>G	NP_000155.1:p.Gln329=
NM_000164.3:c.987A>G	NP_000155.1:p.Gln329=
NM_001308418.1:c.879A>G	NP_001295347.1:p.Gln293=
XM_011526709.1:c.1113A>G	XP_011525011.1:p.Gln371=
XM_011526710.1:c.1113A>G	XP_011525012.1:p.Gln371=
XM_011526711.1:c.1005A>G	XP_011525013.1:p.Gln335=
XM_011526712.1:c.879A>G	XP_011525014.1:p.Gln293=
XM_011526713.1:c.864A>G	XP_011525015.1:p.Gln288=
XM_011526714.1:c.696A>G	XP_011525016.1:p.Gln232=
XM_011526715.1:c.696A>G	XP_011525017.1:p.Gln232=
XM_011526716.1:c.*71A>G	XP_011525018.1:n.*71A>G
XM_011526717.1:c.*71A>G	XP_011525019.1:n.*71A>G
XR_935791.1:n.1006A>G
XM_011526709.2:c.1113A>G	XP_011525011.1:p.Gln371=
XM_011526710.2:c.1113A>G	XP_011525012.1:p.Gln371=
XM_011526711.2:c.1005A>G	XP_011525013.1:p.Gln335=
XM_011526713.2:c.864A>G	XP_011525015.1:p.Gln288=
XM_011526714.2:c.696A>G	XP_011525016.1:p.Gln232=
XM_011526715.2:c.696A>G	XP_011525017.1:p.Gln232=
XM_011526716.2:c.*71A>G	XP_011525018.1:n.*71A>G
XM_017026584.1:c.642A>G	XP_016882073.1:p.Gln214=
XM_017026585.1:c.621A>G	XP_016882074.1:p.Gln207=
XM_017026586.1:c.498A>G	XP_016882075.1:p.Gln166=
XM_017026587.1:c.495A>G	XP_016882076.1:p.Gln165=
XR_001753655.1:n.1082A>G
XR_935791.2:n.1012A>G
NM_000164.4:c.987A>G MANE Select	NP_000155.1:p.Gln329=
NM_001308418.2:c.879A>G	NP_001295347.1:p.Gln293=