Canonical Allele Identifier: CA406395088

Gene: GIPR

Linked Data

• COSMIC: COSM998262
• MyVariant Identifiers: chr19:g.46181200C>G (hg19) ; chr19:g.45677942C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677942C>G , CM000681.2:g.45677942C>G	GRCh38
NC_000019.9:g.46181200C>G , CM000681.1:g.46181200C>G	GRCh37
NC_000019.8:g.50873040C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.961C>G MANE Select	ENSP00000467494.1:p.Leu321Val
ENST00000652180.1:c.778C>G	ENSP00000498426.1:p.Leu260Val
ENST00000263281.7:c.961C>G	ENSP00000263281.3:p.Leu321Val
ENST00000304207.12:c.853C>G	ENSP00000305321.8:p.Leu285Val
ENST00000585889.1:c.*32C>G	ENSP00000467342.1:n.*32C>G
ENST00000590918.5:c.961C>G	ENSP00000467494.1:p.Leu321Val
ENST00000591224.1:n.417C>G
ENST00000593127.1:n.62C>G
NM_000164.2:c.961C>G	NP_000155.1:p.Leu321Val
NM_000164.3:c.961C>G	NP_000155.1:p.Leu321Val
NM_001308418.1:c.853C>G	NP_001295347.1:p.Leu285Val
XM_011526709.1:c.1087C>G	XP_011525011.1:p.Leu363Val
XM_011526710.1:c.1087C>G	XP_011525012.1:p.Leu363Val
XM_011526711.1:c.979C>G	XP_011525013.1:p.Leu327Val
XM_011526712.1:c.853C>G	XP_011525014.1:p.Leu285Val
XM_011526713.1:c.838C>G	XP_011525015.1:p.Leu280Val
XM_011526714.1:c.670C>G	XP_011525016.1:p.Leu224Val
XM_011526715.1:c.670C>G	XP_011525017.1:p.Leu224Val
XM_011526716.1:c.*45C>G	XP_011525018.1:n.*45C>G
XM_011526717.1:c.*45C>G	XP_011525019.1:n.*45C>G
XR_935791.1:n.980C>G
XM_011526709.2:c.1087C>G	XP_011525011.1:p.Leu363Val
XM_011526710.2:c.1087C>G	XP_011525012.1:p.Leu363Val
XM_011526711.2:c.979C>G	XP_011525013.1:p.Leu327Val
XM_011526713.2:c.838C>G	XP_011525015.1:p.Leu280Val
XM_011526714.2:c.670C>G	XP_011525016.1:p.Leu224Val
XM_011526715.2:c.670C>G	XP_011525017.1:p.Leu224Val
XM_011526716.2:c.*45C>G	XP_011525018.1:n.*45C>G
XM_017026584.1:c.616C>G	XP_016882073.1:p.Leu206Val
XM_017026585.1:c.595C>G	XP_016882074.1:p.Leu199Val
XM_017026586.1:c.472C>G	XP_016882075.1:p.Leu158Val
XM_017026587.1:c.469C>G	XP_016882076.1:p.Leu157Val
XR_001753655.1:n.1056C>G
XR_935791.2:n.986C>G
NM_000164.4:c.961C>G MANE Select	NP_000155.1:p.Leu321Val
NM_001308418.2:c.853C>G	NP_001295347.1:p.Leu285Val