Canonical Allele Identifier: CA383919995

Gene: TAS2R20 TAS2R14 PRR4 PRH1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10997209T>A , CM000674.2:g.10997209T>A	GRCh38
NC_000012.11:g.11149808T>A , CM000674.1:g.11149808T>A	GRCh37
NC_000012.10:g.11041075T>A	NCBI36
NG_051254.1:g.6096A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_176889.4:c.667A>T (TAS2R20) MANE Select	NP_795370.2:p.Ile223Phe
ENST00000538986.2:c.667A>T (TAS2R20) MANE Select	ENSP00000441624.1:p.Ile223Phe
NM_001291314.1:c.-125-23488A>T (PRH1)	NP_001278243.1:n.-125-23488A>T
NM_001291314.2:c.-125-23488A>T (PRH1)	NP_001278243.1:n.-125-23488A>T
NM_001291315.1:c.37-23488A>T (PRH1)	NP_001278244.1:n.37-23488A>T
NM_001291315.2:c.37-23488A>T (PRH1)	NP_001278244.1:n.37-23488A>T
NM_001316893.1:c.141-23488A>T	NP_001303822.1:n.141-23488A>T
NM_001316893.2:c.141-23488A>T	NP_001303822.1:n.141-23488A>T
NM_176889.2:c.667A>T (TAS2R20)	NP_795370.2:p.Ile223Phe
NM_176889.3:c.667A>T (TAS2R20)	NP_795370.2:p.Ile223Phe
NR_037918.2:n.478-23488A>T
NR_133575.1:n.372-23488A>T (PRH1)
NR_133575.2:n.360-23488A>T (PRH1)
ENST00000381852.4:n.426-23488A>T (TAS2R14)
ENST00000534923.1:n.96-23488A>T (PRR4)
ENST00000535024.5:c.37-23488A>T (PRR4)	ENSP00000481571.1:n.37-23488A>T
ENST00000535024.6:c.37-23488A>T	ENSP00000481571.2:n.37-23488A>T
ENST00000536086.2:n.23-23488A>T (PRH1)
ENST00000536668.2:c.110-23488A>T	ENSP00000482961.1:n.110-23488A>T
ENST00000538986.1:c.667A>T (TAS2R20)	ENSP00000441624.1:p.Ile223Phe
ENST00000539853.5:c.-125-23488A>T (PRH1)	ENSP00000482068.1:n.-125-23488A>T
ENST00000541977.5:n.293-23488A>T (PRH1)
ENST00000703543.1:c.-125-23488A>T	ENSP00000515364.1:n.-125-23488A>T