Canonical Allele Identifier: CA232917529

Gene: TAS2R14 PRR4 PRH1 TAS2R43

Linked Data

• dbSNP Id: rs79043256
• gnomAD v2: 12-11278999-G-C
• gnomAD v3: 12-11126400-G-C
• gnomAD v4: 12-11126400-G-C
• MyVariant Identifiers: chr12:g.11278999G>C (hg19) ; chr12:g.11126400G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11126400G>C , CM000674.2:g.11126400G>C	GRCh38
NC_000012.11:g.11278999G>C , CM000674.1:g.11278999G>C	GRCh37
NC_000012.10:g.11170266G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000535024.6:c.-134+45022C>G	ENSP00000481571.2:n.-134+45022C>G
ENST00000381852.4:n.152+45022C>G (TAS2R14)
ENST00000535024.5:c.-134+45022C>G (PRR4)	ENSP00000481571.1:n.-134+45022C>G
ENST00000536668.2:c.-165+45022C>G	ENSP00000482961.1:n.-165+45022C>G
ENST00000541175.1:n.40-5220C>G (PRR4)
ENST00000541977.5:n.123+45022C>G (PRH1)
ENST00000546265.1:n.188-5220C>G (PRR4)
ENST00000610639.1:c.87+7758C>G (TAS2R43)	ENSP00000484910.1:n.87+7758C>G
NM_001291314.1:c.-295+45022C>G (PRH1)	NP_001278243.1:n.-295+45022C>G
NM_001291315.1:c.-134+45022C>G (PRH1)	NP_001278244.1:n.-134+45022C>G
NM_001316893.1:c.-134+45022C>G	NP_001303822.1:n.-134+45022C>G
NR_037918.2:n.204+45022C>G
NR_133575.1:n.202+45022C>G (PRH1)
NM_001291314.2:c.-295+45022C>G (PRH1)	NP_001278243.1:n.-295+45022C>G
NM_001291315.2:c.-134+45022C>G (PRH1)	NP_001278244.1:n.-134+45022C>G
NM_001316893.2:c.-134+45022C>G	NP_001303822.1:n.-134+45022C>G
NR_133575.2:n.190+45022C>G (PRH1)