Canonical Allele Identifier: CA406395216

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181235C>G (hg19) ; chr19:g.45677977C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677977C>G , CM000681.2:g.45677977C>G	GRCh38
NC_000019.9:g.46181235C>G , CM000681.1:g.46181235C>G	GRCh37
NC_000019.8:g.50873075C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.996C>G MANE Select	ENSP00000467494.1:p.Cys332Trp
ENST00000652180.1:c.813C>G	ENSP00000498426.1:p.Cys271Trp
ENST00000263281.7:c.996C>G	ENSP00000263281.3:p.Cys332Trp
ENST00000304207.12:c.888C>G	ENSP00000305321.8:p.Cys296Trp
ENST00000585889.1:c.*67C>G	ENSP00000467342.1:n.*67C>G
ENST00000590918.5:c.996C>G	ENSP00000467494.1:p.Cys332Trp
ENST00000591224.1:n.452C>G
ENST00000593127.1:n.97C>G
NM_000164.2:c.996C>G	NP_000155.1:p.Cys332Trp
NM_000164.3:c.996C>G	NP_000155.1:p.Cys332Trp
NM_001308418.1:c.888C>G	NP_001295347.1:p.Cys296Trp
XM_011526709.1:c.1122C>G	XP_011525011.1:p.Cys374Trp
XM_011526710.1:c.1122C>G	XP_011525012.1:p.Cys374Trp
XM_011526711.1:c.1014C>G	XP_011525013.1:p.Cys338Trp
XM_011526712.1:c.888C>G	XP_011525014.1:p.Cys296Trp
XM_011526713.1:c.873C>G	XP_011525015.1:p.Cys291Trp
XM_011526714.1:c.705C>G	XP_011525016.1:p.Cys235Trp
XM_011526715.1:c.705C>G	XP_011525017.1:p.Cys235Trp
XM_011526716.1:c.*80C>G	XP_011525018.1:n.*80C>G
XM_011526717.1:c.*80C>G	XP_011525019.1:n.*80C>G
XR_935791.1:n.1015C>G
XM_011526709.2:c.1122C>G	XP_011525011.1:p.Cys374Trp
XM_011526710.2:c.1122C>G	XP_011525012.1:p.Cys374Trp
XM_011526711.2:c.1014C>G	XP_011525013.1:p.Cys338Trp
XM_011526713.2:c.873C>G	XP_011525015.1:p.Cys291Trp
XM_011526714.2:c.705C>G	XP_011525016.1:p.Cys235Trp
XM_011526715.2:c.705C>G	XP_011525017.1:p.Cys235Trp
XM_011526716.2:c.*80C>G	XP_011525018.1:n.*80C>G
XM_017026584.1:c.651C>G	XP_016882073.1:p.Cys217Trp
XM_017026585.1:c.630C>G	XP_016882074.1:p.Cys210Trp
XM_017026586.1:c.507C>G	XP_016882075.1:p.Cys169Trp
XM_017026587.1:c.504C>G	XP_016882076.1:p.Cys168Trp
XR_001753655.1:n.1091C>G
XR_935791.2:n.1021C>G
NM_000164.4:c.996C>G MANE Select	NP_000155.1:p.Cys332Trp
NM_001308418.2:c.888C>G	NP_001295347.1:p.Cys296Trp