Canonical Allele Identifier: CA2016197603

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10991202C>A , CM000674.2:g.10991202C>A GRCh38
NC_000012.11:g.11143801C>A , CM000674.1:g.11143801C>A GRCh37
NC_000012.10:g.11035068C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000703543.1:c.-125-17481G>T ENSP00000515364.1:n.-125-17481G>T
ENST00000535024.6:c.37-17481G>T ENSP00000481571.2:n.37-17481G>T
ENST00000381852.4:n.426-17481G>T (TAS2R14)
ENST00000534923.1:n.96-17481G>T (PRR4)
ENST00000535024.5:c.37-17481G>T (PRR4) ENSP00000481571.1:n.37-17481G>T
ENST00000536086.2:n.23-17481G>T (PRH1)
ENST00000536668.2:c.110-17481G>T ENSP00000482961.1:n.110-17481G>T
ENST00000539853.5:c.-125-17481G>T (PRH1) ENSP00000482068.1:n.-125-17481G>T
ENST00000541977.5:n.293-17481G>T (PRH1)
NM_001291314.1:c.-125-17481G>T (PRH1) NP_001278243.1:n.-125-17481G>T
NM_001291315.1:c.37-17481G>T (PRH1) NP_001278244.1:n.37-17481G>T
NM_001316893.1:c.141-17481G>T NP_001303822.1:n.141-17481G>T
NR_037918.2:n.478-17481G>T
NR_133575.1:n.372-17481G>T (PRH1)
NM_001291314.2:c.-125-17481G>T (PRH1) NP_001278243.1:n.-125-17481G>T
NM_001291315.2:c.37-17481G>T (PRH1) NP_001278244.1:n.37-17481G>T
NM_001316893.2:c.141-17481G>T NP_001303822.1:n.141-17481G>T
NR_133575.2:n.360-17481G>T (PRH1)