Canonical Allele Identifier: CA406395172

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181224C>G (hg19) ; chr19:g.45677966C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677966C>G , CM000681.2:g.45677966C>G	GRCh38
NC_000019.9:g.46181224C>G , CM000681.1:g.46181224C>G	GRCh37
NC_000019.8:g.50873064C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.985C>G MANE Select	ENSP00000467494.1:p.Gln329Glu
ENST00000652180.1:c.802C>G	ENSP00000498426.1:p.Gln268Glu
ENST00000263281.7:c.985C>G	ENSP00000263281.3:p.Gln329Glu
ENST00000304207.12:c.877C>G	ENSP00000305321.8:p.Gln293Glu
ENST00000585889.1:c.*56C>G	ENSP00000467342.1:n.*56C>G
ENST00000590918.5:c.985C>G	ENSP00000467494.1:p.Gln329Glu
ENST00000591224.1:n.441C>G
ENST00000593127.1:n.86C>G
NM_000164.2:c.985C>G	NP_000155.1:p.Gln329Glu
NM_000164.3:c.985C>G	NP_000155.1:p.Gln329Glu
NM_001308418.1:c.877C>G	NP_001295347.1:p.Gln293Glu
XM_011526709.1:c.1111C>G	XP_011525011.1:p.Gln371Glu
XM_011526710.1:c.1111C>G	XP_011525012.1:p.Gln371Glu
XM_011526711.1:c.1003C>G	XP_011525013.1:p.Gln335Glu
XM_011526712.1:c.877C>G	XP_011525014.1:p.Gln293Glu
XM_011526713.1:c.862C>G	XP_011525015.1:p.Gln288Glu
XM_011526714.1:c.694C>G	XP_011525016.1:p.Gln232Glu
XM_011526715.1:c.694C>G	XP_011525017.1:p.Gln232Glu
XM_011526716.1:c.*69C>G	XP_011525018.1:n.*69C>G
XM_011526717.1:c.*69C>G	XP_011525019.1:n.*69C>G
XR_935791.1:n.1004C>G
XM_011526709.2:c.1111C>G	XP_011525011.1:p.Gln371Glu
XM_011526710.2:c.1111C>G	XP_011525012.1:p.Gln371Glu
XM_011526711.2:c.1003C>G	XP_011525013.1:p.Gln335Glu
XM_011526713.2:c.862C>G	XP_011525015.1:p.Gln288Glu
XM_011526714.2:c.694C>G	XP_011525016.1:p.Gln232Glu
XM_011526715.2:c.694C>G	XP_011525017.1:p.Gln232Glu
XM_011526716.2:c.*69C>G	XP_011525018.1:n.*69C>G
XM_017026584.1:c.640C>G	XP_016882073.1:p.Gln214Glu
XM_017026585.1:c.619C>G	XP_016882074.1:p.Gln207Glu
XM_017026586.1:c.496C>G	XP_016882075.1:p.Gln166Glu
XM_017026587.1:c.493C>G	XP_016882076.1:p.Gln165Glu
XR_001753655.1:n.1080C>G
XR_935791.2:n.1010C>G
NM_000164.4:c.985C>G MANE Select	NP_000155.1:p.Gln329Glu
NM_001308418.2:c.877C>G	NP_001295347.1:p.Gln293Glu