Canonical Allele Identifier: CA507825106

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181199T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677941T>C , CM000681.2:g.45677941T>C	GRCh38
NC_000019.9:g.46181199T>C , CM000681.1:g.46181199T>C	GRCh37
NC_000019.8:g.50873039T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.960T>C MANE Select	ENSP00000467494.1:p.Ile320=
ENST00000652180.1:c.777T>C	ENSP00000498426.1:p.Ile259=
ENST00000263281.7:c.960T>C	ENSP00000263281.3:p.Ile320=
ENST00000304207.12:c.852T>C	ENSP00000305321.8:p.Ile284=
ENST00000585889.1:c.*31T>C	ENSP00000467342.1:n.*31T>C
ENST00000590918.5:c.960T>C	ENSP00000467494.1:p.Ile320=
ENST00000591224.1:n.416T>C
ENST00000593127.1:n.61T>C
NM_000164.2:c.960T>C	NP_000155.1:p.Ile320=
NM_000164.3:c.960T>C	NP_000155.1:p.Ile320=
NM_001308418.1:c.852T>C	NP_001295347.1:p.Ile284=
XM_011526709.1:c.1086T>C	XP_011525011.1:p.Ile362=
XM_011526710.1:c.1086T>C	XP_011525012.1:p.Ile362=
XM_011526711.1:c.978T>C	XP_011525013.1:p.Ile326=
XM_011526712.1:c.852T>C	XP_011525014.1:p.Ile284=
XM_011526713.1:c.837T>C	XP_011525015.1:p.Ile279=
XM_011526714.1:c.669T>C	XP_011525016.1:p.Ile223=
XM_011526715.1:c.669T>C	XP_011525017.1:p.Ile223=
XM_011526716.1:c.*44T>C	XP_011525018.1:n.*44T>C
XM_011526717.1:c.*44T>C	XP_011525019.1:n.*44T>C
XR_935791.1:n.979T>C
XM_011526709.2:c.1086T>C	XP_011525011.1:p.Ile362=
XM_011526710.2:c.1086T>C	XP_011525012.1:p.Ile362=
XM_011526711.2:c.978T>C	XP_011525013.1:p.Ile326=
XM_011526713.2:c.837T>C	XP_011525015.1:p.Ile279=
XM_011526714.2:c.669T>C	XP_011525016.1:p.Ile223=
XM_011526715.2:c.669T>C	XP_011525017.1:p.Ile223=
XM_011526716.2:c.*44T>C	XP_011525018.1:n.*44T>C
XM_017026584.1:c.615T>C	XP_016882073.1:p.Ile205=
XM_017026585.1:c.594T>C	XP_016882074.1:p.Ile198=
XM_017026586.1:c.471T>C	XP_016882075.1:p.Ile157=
XM_017026587.1:c.468T>C	XP_016882076.1:p.Ile156=
XR_001753655.1:n.1055T>C
XR_935791.2:n.985T>C
NM_000164.4:c.960T>C MANE Select	NP_000155.1:p.Ile320=
NM_001308418.2:c.852T>C	NP_001295347.1:p.Ile284=