Canonical Allele Identifier: CA406395106

Gene: GIPR

Linked Data

• gnomAD v4: 19-45677946-T-G
• MyVariant Identifiers: chr19:g.46181204T>G (hg19) ; chr19:g.45677946T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677946T>G , CM000681.2:g.45677946T>G	GRCh38
NC_000019.9:g.46181204T>G , CM000681.1:g.46181204T>G	GRCh37
NC_000019.8:g.50873044T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.965T>G MANE Select	ENSP00000467494.1:p.Leu322Arg
ENST00000652180.1:c.782T>G	ENSP00000498426.1:p.Leu261Arg
ENST00000263281.7:c.965T>G	ENSP00000263281.3:p.Leu322Arg
ENST00000304207.12:c.857T>G	ENSP00000305321.8:p.Leu286Arg
ENST00000585889.1:c.*36T>G	ENSP00000467342.1:n.*36T>G
ENST00000590918.5:c.965T>G	ENSP00000467494.1:p.Leu322Arg
ENST00000591224.1:n.421T>G
ENST00000593127.1:n.66T>G
NM_000164.2:c.965T>G	NP_000155.1:p.Leu322Arg
NM_000164.3:c.965T>G	NP_000155.1:p.Leu322Arg
NM_001308418.1:c.857T>G	NP_001295347.1:p.Leu286Arg
XM_011526709.1:c.1091T>G	XP_011525011.1:p.Leu364Arg
XM_011526710.1:c.1091T>G	XP_011525012.1:p.Leu364Arg
XM_011526711.1:c.983T>G	XP_011525013.1:p.Leu328Arg
XM_011526712.1:c.857T>G	XP_011525014.1:p.Leu286Arg
XM_011526713.1:c.842T>G	XP_011525015.1:p.Leu281Arg
XM_011526714.1:c.674T>G	XP_011525016.1:p.Leu225Arg
XM_011526715.1:c.674T>G	XP_011525017.1:p.Leu225Arg
XM_011526716.1:c.*49T>G	XP_011525018.1:n.*49T>G
XM_011526717.1:c.*49T>G	XP_011525019.1:n.*49T>G
XR_935791.1:n.984T>G
XM_011526709.2:c.1091T>G	XP_011525011.1:p.Leu364Arg
XM_011526710.2:c.1091T>G	XP_011525012.1:p.Leu364Arg
XM_011526711.2:c.983T>G	XP_011525013.1:p.Leu328Arg
XM_011526713.2:c.842T>G	XP_011525015.1:p.Leu281Arg
XM_011526714.2:c.674T>G	XP_011525016.1:p.Leu225Arg
XM_011526715.2:c.674T>G	XP_011525017.1:p.Leu225Arg
XM_011526716.2:c.*49T>G	XP_011525018.1:n.*49T>G
XM_017026584.1:c.620T>G	XP_016882073.1:p.Leu207Arg
XM_017026585.1:c.599T>G	XP_016882074.1:p.Leu200Arg
XM_017026586.1:c.476T>G	XP_016882075.1:p.Leu159Arg
XM_017026587.1:c.473T>G	XP_016882076.1:p.Leu158Arg
XR_001753655.1:n.1060T>G
XR_935791.2:n.990T>G
NM_000164.4:c.965T>G MANE Select	NP_000155.1:p.Leu322Arg
NM_001308418.2:c.857T>G	NP_001295347.1:p.Leu286Arg