Canonical Allele Identifier: CA2838370150

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.11131476A>T , CM000674.2:g.11131476A>T GRCh38
NC_000012.11:g.11284075A>T , CM000674.1:g.11284075A>T GRCh37
NC_000012.10:g.11175342A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000535024.6:c.-134+39946T>A ENSP00000481571.2:n.-134+39946T>A
ENST00000381852.4:n.152+39946T>A (TAS2R14)
ENST00000535024.5:c.-134+39946T>A (PRR4) ENSP00000481571.1:n.-134+39946T>A
ENST00000536668.2:c.-165+39946T>A ENSP00000482961.1:n.-165+39946T>A
ENST00000541175.1:n.40-10296T>A (PRR4)
ENST00000541977.5:n.123+39946T>A (PRH1)
ENST00000546265.1:n.188-10296T>A (PRR4)
ENST00000610639.1:c.87+2682T>A (TAS2R43) ENSP00000484910.1:n.87+2682T>A
NM_001291314.1:c.-295+39946T>A (PRH1) NP_001278243.1:n.-295+39946T>A
NM_001291315.1:c.-134+39946T>A (PRH1) NP_001278244.1:n.-134+39946T>A
NM_001316893.1:c.-134+39946T>A NP_001303822.1:n.-134+39946T>A
NR_037918.2:n.204+39946T>A
NR_133575.1:n.202+39946T>A (PRH1)
NM_001291314.2:c.-295+39946T>A (PRH1) NP_001278243.1:n.-295+39946T>A
NM_001291315.2:c.-134+39946T>A (PRH1) NP_001278244.1:n.-134+39946T>A
NM_001316893.2:c.-134+39946T>A NP_001303822.1:n.-134+39946T>A
NR_133575.2:n.190+39946T>A (PRH1)