Canonical Allele Identifier: CA2016268757

Gene: TAS2R14 PRR4 PRH1 TAS2R43

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11126493C= , CM000674.2:g.11126493C=	GRCh38
NC_000012.11:g.11279092C= , CM000674.1:g.11279092C=	GRCh37
NC_000012.10:g.11170359C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001291314.1:c.-295+44929G= (PRH1)	NP_001278243.1:n.-295+44929G=
NM_001291314.2:c.-295+44929G= (PRH1)	NP_001278243.1:n.-295+44929G=
NM_001291315.1:c.-134+44929G= (PRH1)	NP_001278244.1:n.-134+44929G=
NM_001291315.2:c.-134+44929G= (PRH1)	NP_001278244.1:n.-134+44929G=
NM_001316893.1:c.-134+44929G=	NP_001303822.1:n.-134+44929G=
NM_001316893.2:c.-134+44929G=	NP_001303822.1:n.-134+44929G=
NR_037918.2:n.204+44929G=
NR_133575.1:n.202+44929G= (PRH1)
NR_133575.2:n.190+44929G= (PRH1)
ENST00000381852.4:n.152+44929G= (TAS2R14)
ENST00000535024.5:c.-134+44929G= (PRR4)	ENSP00000481571.1:n.-134+44929G=
ENST00000535024.6:c.-134+44929G=	ENSP00000481571.2:n.-134+44929G=
ENST00000536668.2:c.-165+44929G=	ENSP00000482961.1:n.-165+44929G=
ENST00000541175.1:n.40-5313G= (PRR4)
ENST00000541977.5:n.123+44929G= (PRH1)
ENST00000546265.1:n.188-5313G= (PRR4)
ENST00000610639.1:c.87+7665G= (TAS2R43)	ENSP00000484910.1:n.87+7665G=