Canonical Allele Identifier: CA308987458

Gene: GIPR

Linked Data

• dbSNP Id: rs375292744
• gnomAD v4: 19-45677963-C-G
• MyVariant Identifiers: chr19:g.46181221C>G (hg19) ; chr19:g.45677963C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677963C>G , CM000681.2:g.45677963C>G	GRCh38
NC_000019.9:g.46181221C>G , CM000681.1:g.46181221C>G	GRCh37
NC_000019.8:g.50873061C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.982C>G MANE Select	ENSP00000467494.1:p.Arg328Gly
ENST00000652180.1:c.799C>G	ENSP00000498426.1:p.Arg267Gly
ENST00000263281.7:c.982C>G	ENSP00000263281.3:p.Arg328Gly
ENST00000304207.12:c.874C>G	ENSP00000305321.8:p.Arg292Gly
ENST00000585889.1:c.*53C>G	ENSP00000467342.1:n.*53C>G
ENST00000590918.5:c.982C>G	ENSP00000467494.1:p.Arg328Gly
ENST00000591224.1:n.438C>G
ENST00000593127.1:n.83C>G
NM_000164.2:c.982C>G	NP_000155.1:p.Arg328Gly
NM_000164.3:c.982C>G	NP_000155.1:p.Arg328Gly
NM_001308418.1:c.874C>G	NP_001295347.1:p.Arg292Gly
XM_011526709.1:c.1108C>G	XP_011525011.1:p.Arg370Gly
XM_011526710.1:c.1108C>G	XP_011525012.1:p.Arg370Gly
XM_011526711.1:c.1000C>G	XP_011525013.1:p.Arg334Gly
XM_011526712.1:c.874C>G	XP_011525014.1:p.Arg292Gly
XM_011526713.1:c.859C>G	XP_011525015.1:p.Arg287Gly
XM_011526714.1:c.691C>G	XP_011525016.1:p.Arg231Gly
XM_011526715.1:c.691C>G	XP_011525017.1:p.Arg231Gly
XM_011526716.1:c.*66C>G	XP_011525018.1:n.*66C>G
XM_011526717.1:c.*66C>G	XP_011525019.1:n.*66C>G
XR_935791.1:n.1001C>G
XM_011526709.2:c.1108C>G	XP_011525011.1:p.Arg370Gly
XM_011526710.2:c.1108C>G	XP_011525012.1:p.Arg370Gly
XM_011526711.2:c.1000C>G	XP_011525013.1:p.Arg334Gly
XM_011526713.2:c.859C>G	XP_011525015.1:p.Arg287Gly
XM_011526714.2:c.691C>G	XP_011525016.1:p.Arg231Gly
XM_011526715.2:c.691C>G	XP_011525017.1:p.Arg231Gly
XM_011526716.2:c.*66C>G	XP_011525018.1:n.*66C>G
XM_017026584.1:c.637C>G	XP_016882073.1:p.Arg213Gly
XM_017026585.1:c.616C>G	XP_016882074.1:p.Arg206Gly
XM_017026586.1:c.493C>G	XP_016882075.1:p.Arg165Gly
XM_017026587.1:c.490C>G	XP_016882076.1:p.Arg164Gly
XR_001753655.1:n.1077C>G
XR_935791.2:n.1007C>G
NM_000164.4:c.982C>G MANE Select	NP_000155.1:p.Arg328Gly
NM_001308418.2:c.874C>G	NP_001295347.1:p.Arg292Gly