Canonical Allele Identifier: CA507825118

Gene: GIPR

Linked Data

• MyVariant Identifiers: chr19:g.46181214G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45677956G>T , CM000681.2:g.45677956G>T	GRCh38
NC_000019.9:g.46181214G>T , CM000681.1:g.46181214G>T	GRCh37
NC_000019.8:g.50873054G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590918.6:c.975G>T MANE Select	ENSP00000467494.1:p.Leu325=
ENST00000652180.1:c.792G>T	ENSP00000498426.1:p.Leu264=
ENST00000263281.7:c.975G>T	ENSP00000263281.3:p.Leu325=
ENST00000304207.12:c.867G>T	ENSP00000305321.8:p.Leu289=
ENST00000585889.1:c.*46G>T	ENSP00000467342.1:n.*46G>T
ENST00000590918.5:c.975G>T	ENSP00000467494.1:p.Leu325=
ENST00000591224.1:n.431G>T
ENST00000593127.1:n.76G>T
NM_000164.2:c.975G>T	NP_000155.1:p.Leu325=
NM_000164.3:c.975G>T	NP_000155.1:p.Leu325=
NM_001308418.1:c.867G>T	NP_001295347.1:p.Leu289=
XM_011526709.1:c.1101G>T	XP_011525011.1:p.Leu367=
XM_011526710.1:c.1101G>T	XP_011525012.1:p.Leu367=
XM_011526711.1:c.993G>T	XP_011525013.1:p.Leu331=
XM_011526712.1:c.867G>T	XP_011525014.1:p.Leu289=
XM_011526713.1:c.852G>T	XP_011525015.1:p.Leu284=
XM_011526714.1:c.684G>T	XP_011525016.1:p.Leu228=
XM_011526715.1:c.684G>T	XP_011525017.1:p.Leu228=
XM_011526716.1:c.*59G>T	XP_011525018.1:n.*59G>T
XM_011526717.1:c.*59G>T	XP_011525019.1:n.*59G>T
XR_935791.1:n.994G>T
XM_011526709.2:c.1101G>T	XP_011525011.1:p.Leu367=
XM_011526710.2:c.1101G>T	XP_011525012.1:p.Leu367=
XM_011526711.2:c.993G>T	XP_011525013.1:p.Leu331=
XM_011526713.2:c.852G>T	XP_011525015.1:p.Leu284=
XM_011526714.2:c.684G>T	XP_011525016.1:p.Leu228=
XM_011526715.2:c.684G>T	XP_011525017.1:p.Leu228=
XM_011526716.2:c.*59G>T	XP_011525018.1:n.*59G>T
XM_017026584.1:c.630G>T	XP_016882073.1:p.Leu210=
XM_017026585.1:c.609G>T	XP_016882074.1:p.Leu203=
XM_017026586.1:c.486G>T	XP_016882075.1:p.Leu162=
XM_017026587.1:c.483G>T	XP_016882076.1:p.Leu161=
XR_001753655.1:n.1070G>T
XR_935791.2:n.1000G>T
NM_000164.4:c.975G>T MANE Select	NP_000155.1:p.Leu325=
NM_001308418.2:c.867G>T	NP_001295347.1:p.Leu289=