Canonical Allele Identifier: CA406395137

Gene: GIPR

Linked Data

• dbSNP Id: rs1242475885
• gnomAD v2: 19-46181213-T-G
• gnomAD v4: 19-45677955-T-G
• MyVariant Identifiers: chr19:g.46181213T>G (hg19) ; chr19:g.45677955T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677955T>G , CM000681.2:g.45677955T>G	GRCh38
NC_000019.9:g.46181213T>G , CM000681.1:g.46181213T>G	GRCh37
NC_000019.8:g.50873053T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.974T>G MANE Select	ENSP00000467494.1:p.Leu325Arg
ENST00000652180.1:c.791T>G	ENSP00000498426.1:p.Leu264Arg
ENST00000263281.7:c.974T>G	ENSP00000263281.3:p.Leu325Arg
ENST00000304207.12:c.866T>G	ENSP00000305321.8:p.Leu289Arg
ENST00000585889.1:c.*45T>G	ENSP00000467342.1:n.*45T>G
ENST00000590918.5:c.974T>G	ENSP00000467494.1:p.Leu325Arg
ENST00000591224.1:n.430T>G
ENST00000593127.1:n.75T>G
NM_000164.2:c.974T>G	NP_000155.1:p.Leu325Arg
NM_000164.3:c.974T>G	NP_000155.1:p.Leu325Arg
NM_001308418.1:c.866T>G	NP_001295347.1:p.Leu289Arg
XM_011526709.1:c.1100T>G	XP_011525011.1:p.Leu367Arg
XM_011526710.1:c.1100T>G	XP_011525012.1:p.Leu367Arg
XM_011526711.1:c.992T>G	XP_011525013.1:p.Leu331Arg
XM_011526712.1:c.866T>G	XP_011525014.1:p.Leu289Arg
XM_011526713.1:c.851T>G	XP_011525015.1:p.Leu284Arg
XM_011526714.1:c.683T>G	XP_011525016.1:p.Leu228Arg
XM_011526715.1:c.683T>G	XP_011525017.1:p.Leu228Arg
XM_011526716.1:c.*58T>G	XP_011525018.1:n.*58T>G
XM_011526717.1:c.*58T>G	XP_011525019.1:n.*58T>G
XR_935791.1:n.993T>G
XM_011526709.2:c.1100T>G	XP_011525011.1:p.Leu367Arg
XM_011526710.2:c.1100T>G	XP_011525012.1:p.Leu367Arg
XM_011526711.2:c.992T>G	XP_011525013.1:p.Leu331Arg
XM_011526713.2:c.851T>G	XP_011525015.1:p.Leu284Arg
XM_011526714.2:c.683T>G	XP_011525016.1:p.Leu228Arg
XM_011526715.2:c.683T>G	XP_011525017.1:p.Leu228Arg
XM_011526716.2:c.*58T>G	XP_011525018.1:n.*58T>G
XM_017026584.1:c.629T>G	XP_016882073.1:p.Leu210Arg
XM_017026585.1:c.608T>G	XP_016882074.1:p.Leu203Arg
XM_017026586.1:c.485T>G	XP_016882075.1:p.Leu162Arg
XM_017026587.1:c.482T>G	XP_016882076.1:p.Leu161Arg
XR_001753655.1:n.1069T>G
XR_935791.2:n.999T>G
NM_000164.4:c.974T>G MANE Select	NP_000155.1:p.Leu325Arg
NM_001308418.2:c.866T>G	NP_001295347.1:p.Leu289Arg