Canonical Allele Identifier: CA406395236

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181240A>G (hg19) ; chr19:g.45677982A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677982A>G , CM000681.2:g.45677982A>G	GRCh38
NC_000019.9:g.46181240A>G , CM000681.1:g.46181240A>G	GRCh37
NC_000019.8:g.50873080A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1001A>G MANE Select	ENSP00000467494.1:p.Asp334Gly
ENST00000652180.1:c.818A>G	ENSP00000498426.1:p.Asp273Gly
ENST00000263281.7:c.1001A>G	ENSP00000263281.3:p.Asp334Gly
ENST00000304207.12:c.893A>G	ENSP00000305321.8:p.Asp298Gly
ENST00000585889.1:c.*72A>G	ENSP00000467342.1:n.*72A>G
ENST00000590918.5:c.1001A>G	ENSP00000467494.1:p.Asp334Gly
ENST00000591224.1:n.457A>G
ENST00000593127.1:n.102A>G
NM_000164.2:c.1001A>G	NP_000155.1:p.Asp334Gly
NM_000164.3:c.1001A>G	NP_000155.1:p.Asp334Gly
NM_001308418.1:c.893A>G	NP_001295347.1:p.Asp298Gly
XM_011526709.1:c.1127A>G	XP_011525011.1:p.Asp376Gly
XM_011526710.1:c.1127A>G	XP_011525012.1:p.Asp376Gly
XM_011526711.1:c.1019A>G	XP_011525013.1:p.Asp340Gly
XM_011526712.1:c.893A>G	XP_011525014.1:p.Asp298Gly
XM_011526713.1:c.878A>G	XP_011525015.1:p.Asp293Gly
XM_011526714.1:c.710A>G	XP_011525016.1:p.Asp237Gly
XM_011526715.1:c.710A>G	XP_011525017.1:p.Asp237Gly
XM_011526716.1:c.*85A>G	XP_011525018.1:n.*85A>G
XM_011526717.1:c.*85A>G	XP_011525019.1:n.*85A>G
XR_935791.1:n.1020A>G
XM_011526709.2:c.1127A>G	XP_011525011.1:p.Asp376Gly
XM_011526710.2:c.1127A>G	XP_011525012.1:p.Asp376Gly
XM_011526711.2:c.1019A>G	XP_011525013.1:p.Asp340Gly
XM_011526713.2:c.878A>G	XP_011525015.1:p.Asp293Gly
XM_011526714.2:c.710A>G	XP_011525016.1:p.Asp237Gly
XM_011526715.2:c.710A>G	XP_011525017.1:p.Asp237Gly
XM_011526716.2:c.*85A>G	XP_011525018.1:n.*85A>G
XM_017026584.1:c.656A>G	XP_016882073.1:p.Asp219Gly
XM_017026585.1:c.635A>G	XP_016882074.1:p.Asp212Gly
XM_017026586.1:c.512A>G	XP_016882075.1:p.Asp171Gly
XM_017026587.1:c.509A>G	XP_016882076.1:p.Asp170Gly
XR_001753655.1:n.1096A>G
XR_935791.2:n.1026A>G
NM_000164.4:c.1001A>G MANE Select	NP_000155.1:p.Asp334Gly
NM_001308418.2:c.893A>G	NP_001295347.1:p.Asp298Gly