Canonical Allele Identifier: CA406395241

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181241T>G (hg19) ; chr19:g.45677983T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677983T>G , CM000681.2:g.45677983T>G	GRCh38
NC_000019.9:g.46181241T>G , CM000681.1:g.46181241T>G	GRCh37
NC_000019.8:g.50873081T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1002T>G MANE Select	ENSP00000467494.1:p.Asp334Glu
ENST00000652180.1:c.819T>G	ENSP00000498426.1:p.Asp273Glu
ENST00000263281.7:c.1002T>G	ENSP00000263281.3:p.Asp334Glu
ENST00000304207.12:c.894T>G	ENSP00000305321.8:p.Asp298Glu
ENST00000585889.1:c.*73T>G	ENSP00000467342.1:n.*73T>G
ENST00000590918.5:c.1002T>G	ENSP00000467494.1:p.Asp334Glu
ENST00000591224.1:n.458T>G
ENST00000593127.1:n.103T>G
NM_000164.2:c.1002T>G	NP_000155.1:p.Asp334Glu
NM_000164.3:c.1002T>G	NP_000155.1:p.Asp334Glu
NM_001308418.1:c.894T>G	NP_001295347.1:p.Asp298Glu
XM_011526709.1:c.1128T>G	XP_011525011.1:p.Asp376Glu
XM_011526710.1:c.1128T>G	XP_011525012.1:p.Asp376Glu
XM_011526711.1:c.1020T>G	XP_011525013.1:p.Asp340Glu
XM_011526712.1:c.894T>G	XP_011525014.1:p.Asp298Glu
XM_011526713.1:c.879T>G	XP_011525015.1:p.Asp293Glu
XM_011526714.1:c.711T>G	XP_011525016.1:p.Asp237Glu
XM_011526715.1:c.711T>G	XP_011525017.1:p.Asp237Glu
XM_011526716.1:c.*86T>G	XP_011525018.1:n.*86T>G
XM_011526717.1:c.*86T>G	XP_011525019.1:n.*86T>G
XR_935791.1:n.1021T>G
XM_011526709.2:c.1128T>G	XP_011525011.1:p.Asp376Glu
XM_011526710.2:c.1128T>G	XP_011525012.1:p.Asp376Glu
XM_011526711.2:c.1020T>G	XP_011525013.1:p.Asp340Glu
XM_011526713.2:c.879T>G	XP_011525015.1:p.Asp293Glu
XM_011526714.2:c.711T>G	XP_011525016.1:p.Asp237Glu
XM_011526715.2:c.711T>G	XP_011525017.1:p.Asp237Glu
XM_011526716.2:c.*86T>G	XP_011525018.1:n.*86T>G
XM_017026584.1:c.657T>G	XP_016882073.1:p.Asp219Glu
XM_017026585.1:c.636T>G	XP_016882074.1:p.Asp212Glu
XM_017026586.1:c.513T>G	XP_016882075.1:p.Asp171Glu
XM_017026587.1:c.510T>G	XP_016882076.1:p.Asp170Glu
XR_001753655.1:n.1097T>G
XR_935791.2:n.1027T>G
NM_000164.4:c.1002T>G MANE Select	NP_000155.1:p.Asp334Glu
NM_001308418.2:c.894T>G	NP_001295347.1:p.Asp298Glu