Canonical Allele Identifier: CA2794546231

Gene: TAS2R14 TAS2R19 PRR4 PRH1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11021677_11021678delinsAC , CM000674.2:g.11021677_11021678delinsAC	GRCh38
NC_000012.11:g.11174276_11174277delinsAC , CM000674.1:g.11174276_11174277delinsAC	GRCh37
NC_000012.10:g.11065543_11065544delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703543.1:c.-126+25342_-126+25343delinsGT	ENSP00000515364.1:n.-126+25342_-126+25343delinsGT
ENST00000535024.6:c.36+25342_36+25343delinsGT	ENSP00000481571.2:n.36+25342_36+25343delinsGT
ENST00000381852.4:n.425+13104_425+13105delinsGT (TAS2R14)
ENST00000390673.2:c.894_895delinsGT (TAS2R19) MANE Select	ENSP00000375091.2:p.Arg299Cys
ENST00000534923.1:n.95+25342_95+25343delinsGT (PRR4)
ENST00000535024.5:c.36+25342_36+25343delinsGT (PRR4)	ENSP00000481571.1:n.36+25342_36+25343delinsGT
ENST00000536086.2:n.22+25342_22+25343delinsGT (PRH1)
ENST00000536668.2:c.109+13104_109+13105delinsGT	ENSP00000482961.1:n.109+13104_109+13105delinsGT
ENST00000539853.5:c.-126+25342_-126+25343delinsGT (PRH1)	ENSP00000482068.1:n.-126+25342_-126+25343delinsGT
ENST00000541456.1:n.119-15409_119-15408delinsGT (PRR4)
ENST00000541977.5:n.292+25342_292+25343delinsGT (PRH1)
NM_001291314.1:c.-126+25342_-126+25343delinsGT (PRH1)	NP_001278243.1:n.-126+25342_-126+25343delinsGT
NM_001291315.1:c.36+25342_36+25343delinsGT (PRH1)	NP_001278244.1:n.36+25342_36+25343delinsGT
NM_001316893.1:c.140+13104_140+13105delinsGT	NP_001303822.1:n.140+13104_140+13105delinsGT
NM_176888.2:c.894_895delinsGT (TAS2R19) MANE Select	NP_795369.1:p.Arg299Cys
NR_037918.2:n.477+13104_477+13105delinsGT
NR_133575.1:n.371+25342_371+25343delinsGT (PRH1)
NM_001291314.2:c.-126+25342_-126+25343delinsGT (PRH1)	NP_001278243.1:n.-126+25342_-126+25343delinsGT
NM_001291315.2:c.36+25342_36+25343delinsGT (PRH1)	NP_001278244.1:n.36+25342_36+25343delinsGT
NM_001316893.2:c.140+13104_140+13105delinsGT	NP_001303822.1:n.140+13104_140+13105delinsGT
NR_133575.2:n.359+25342_359+25343delinsGT (PRH1)