Canonical Allele Identifier: CA232917515

Gene: TAS2R14 PRR4 PRH1 TAS2R43

Linked Data

• dbSNP Id: rs759509676
• MyVariant Identifiers: chr12:g.11278992A>G (hg19) ; chr12:g.11126393A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11126393A>G , CM000674.2:g.11126393A>G	GRCh38
NC_000012.11:g.11278992A>G , CM000674.1:g.11278992A>G	GRCh37
NC_000012.10:g.11170259A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000535024.6:c.-134+45029T>C	ENSP00000481571.2:n.-134+45029T>C
ENST00000381852.4:n.152+45029T>C (TAS2R14)
ENST00000535024.5:c.-134+45029T>C (PRR4)	ENSP00000481571.1:n.-134+45029T>C
ENST00000536668.2:c.-165+45029T>C	ENSP00000482961.1:n.-165+45029T>C
ENST00000541175.1:n.40-5213T>C (PRR4)
ENST00000541977.5:n.123+45029T>C (PRH1)
ENST00000546265.1:n.188-5213T>C (PRR4)
ENST00000610639.1:c.87+7765T>C (TAS2R43)	ENSP00000484910.1:n.87+7765T>C
NM_001291314.1:c.-295+45029T>C (PRH1)	NP_001278243.1:n.-295+45029T>C
NM_001291315.1:c.-134+45029T>C (PRH1)	NP_001278244.1:n.-134+45029T>C
NM_001316893.1:c.-134+45029T>C	NP_001303822.1:n.-134+45029T>C
NR_037918.2:n.204+45029T>C
NR_133575.1:n.202+45029T>C (PRH1)
NM_001291314.2:c.-295+45029T>C (PRH1)	NP_001278243.1:n.-295+45029T>C
NM_001291315.2:c.-134+45029T>C (PRH1)	NP_001278244.1:n.-134+45029T>C
NM_001316893.2:c.-134+45029T>C	NP_001303822.1:n.-134+45029T>C
NR_133575.2:n.190+45029T>C (PRH1)