Canonical Allele Identifier: CA507825153

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181349G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45678091G>T , CM000681.2:g.45678091G>T	GRCh38
NC_000019.9:g.46181349G>T , CM000681.1:g.46181349G>T	GRCh37
NC_000019.8:g.50873189G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.1017G>T MANE Select	ENSP00000467494.1:p.Leu339=
ENST00000652180.1:c.834G>T	ENSP00000498426.1:p.Leu278=
ENST00000263281.7:c.1017G>T	ENSP00000263281.3:p.Leu339=
ENST00000304207.12:c.909G>T	ENSP00000305321.8:p.Leu303=
ENST00000585889.1:c.*88G>T	ENSP00000467342.1:n.*88G>T
ENST00000590918.5:c.1017G>T	ENSP00000467494.1:p.Leu339=
ENST00000591224.1:n.473G>T
ENST00000593127.1:n.118G>T
NM_000164.2:c.1017G>T	NP_000155.1:p.Leu339=
NM_000164.3:c.1017G>T	NP_000155.1:p.Leu339=
NM_001308418.1:c.909G>T	NP_001295347.1:p.Leu303=
XM_011526709.1:c.1143G>T	XP_011525011.1:p.Leu381=
XM_011526710.1:c.1143G>T	XP_011525012.1:p.Leu381=
XM_011526711.1:c.1035G>T	XP_011525013.1:p.Leu345=
XM_011526712.1:c.909G>T	XP_011525014.1:p.Leu303=
XM_011526713.1:c.894G>T	XP_011525015.1:p.Leu298=
XM_011526714.1:c.726G>T	XP_011525016.1:p.Leu242=
XM_011526715.1:c.726G>T	XP_011525017.1:p.Leu242=
XR_935791.1:n.1036G>T
XM_011526709.2:c.1143G>T	XP_011525011.1:p.Leu381=
XM_011526710.2:c.1143G>T	XP_011525012.1:p.Leu381=
XM_011526711.2:c.1035G>T	XP_011525013.1:p.Leu345=
XM_011526713.2:c.894G>T	XP_011525015.1:p.Leu298=
XM_011526714.2:c.726G>T	XP_011525016.1:p.Leu242=
XM_011526715.2:c.726G>T	XP_011525017.1:p.Leu242=
XM_017026584.1:c.672G>T	XP_016882073.1:p.Leu224=
XM_017026585.1:c.651G>T	XP_016882074.1:p.Leu217=
XM_017026586.1:c.528G>T	XP_016882075.1:p.Leu176=
XM_017026587.1:c.525G>T	XP_016882076.1:p.Leu175=
XR_001753655.1:n.1112G>T
XR_935791.2:n.1042G>T
NM_000164.4:c.1017G>T MANE Select	NP_000155.1:p.Leu339=
NM_001308418.2:c.909G>T	NP_001295347.1:p.Leu303=