Canonical Allele Identifier: CA406395209

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181234G>A (hg19) ; chr19:g.45677976G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677976G>A , CM000681.2:g.45677976G>A	GRCh38
NC_000019.9:g.46181234G>A , CM000681.1:g.46181234G>A	GRCh37
NC_000019.8:g.50873074G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.995G>A MANE Select	ENSP00000467494.1:p.Cys332Tyr
ENST00000652180.1:c.812G>A	ENSP00000498426.1:p.Cys271Tyr
ENST00000263281.7:c.995G>A	ENSP00000263281.3:p.Cys332Tyr
ENST00000304207.12:c.887G>A	ENSP00000305321.8:p.Cys296Tyr
ENST00000585889.1:c.*66G>A	ENSP00000467342.1:n.*66G>A
ENST00000590918.5:c.995G>A	ENSP00000467494.1:p.Cys332Tyr
ENST00000591224.1:n.451G>A
ENST00000593127.1:n.96G>A
NM_000164.2:c.995G>A	NP_000155.1:p.Cys332Tyr
NM_000164.3:c.995G>A	NP_000155.1:p.Cys332Tyr
NM_001308418.1:c.887G>A	NP_001295347.1:p.Cys296Tyr
XM_011526709.1:c.1121G>A	XP_011525011.1:p.Cys374Tyr
XM_011526710.1:c.1121G>A	XP_011525012.1:p.Cys374Tyr
XM_011526711.1:c.1013G>A	XP_011525013.1:p.Cys338Tyr
XM_011526712.1:c.887G>A	XP_011525014.1:p.Cys296Tyr
XM_011526713.1:c.872G>A	XP_011525015.1:p.Cys291Tyr
XM_011526714.1:c.704G>A	XP_011525016.1:p.Cys235Tyr
XM_011526715.1:c.704G>A	XP_011525017.1:p.Cys235Tyr
XM_011526716.1:c.*79G>A	XP_011525018.1:n.*79G>A
XM_011526717.1:c.*79G>A	XP_011525019.1:n.*79G>A
XR_935791.1:n.1014G>A
XM_011526709.2:c.1121G>A	XP_011525011.1:p.Cys374Tyr
XM_011526710.2:c.1121G>A	XP_011525012.1:p.Cys374Tyr
XM_011526711.2:c.1013G>A	XP_011525013.1:p.Cys338Tyr
XM_011526713.2:c.872G>A	XP_011525015.1:p.Cys291Tyr
XM_011526714.2:c.704G>A	XP_011525016.1:p.Cys235Tyr
XM_011526715.2:c.704G>A	XP_011525017.1:p.Cys235Tyr
XM_011526716.2:c.*79G>A	XP_011525018.1:n.*79G>A
XM_017026584.1:c.650G>A	XP_016882073.1:p.Cys217Tyr
XM_017026585.1:c.629G>A	XP_016882074.1:p.Cys210Tyr
XM_017026586.1:c.506G>A	XP_016882075.1:p.Cys169Tyr
XM_017026587.1:c.503G>A	XP_016882076.1:p.Cys168Tyr
XR_001753655.1:n.1090G>A
XR_935791.2:n.1020G>A
NM_000164.4:c.995G>A MANE Select	NP_000155.1:p.Cys332Tyr
NM_001308418.2:c.887G>A	NP_001295347.1:p.Cys296Tyr