Canonical Allele Identifier: CA12295153

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43582731G>A , CM000668.2:g.43582731G>A GRCh38
NC_000006.11:g.43550468G>A , CM000668.1:g.43550468G>A GRCh37
NC_000006.10:g.43658446G>A NCBI36
NG_009252.1:g.11591G>A , LRG_470:g.11591G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372236.9:c.138-276G>A (POLH) MANE Select ENSP00000361310.4:n.138-276G>A
ENST00000372226.1:c.138-276G>A (POLH) ENSP00000361300.1:n.138-276G>A
ENST00000372236.8:c.138-276G>A (POLH) ENSP00000361310.4:n.138-276G>A
ENST00000443535.1:c.-49-276G>A (POLH) ENSP00000405320.1:n.-49-276G>A
NM_001291969.1:c.-17-276G>A (POLH) NP_001278898.1:n.-17-276G>A
NM_001291970.1:c.138-276G>A (POLH) NP_001278899.1:n.138-276G>A
NM_006502.2:c.138-276G>A , LRG_470t1:c.138-276G>A (POLH) NP_006493.1:n.138-276G>A
XM_005249186.2:c.-49-276G>A (POLH) XP_005249243.1:n.-49-276G>A
XM_011514698.1:c.-17-276G>A (POLH) XP_011513000.1:n.-17-276G>A
XM_005249186.4:c.-49-276G>A (POLH) XP_005249243.1:n.-49-276G>A
XM_011514698.3:c.-17-276G>A (POLH) XP_011513000.1:n.-17-276G>A
XM_024446466.1:c.-2866-276G>A (POLH) XP_024302234.1:n.-2866-276G>A
XM_024446467.1:c.-482-276G>A (POLH) XP_024302235.1:n.-482-276G>A
NM_001291969.2:c.-17-276G>A (POLH) NP_001278898.1:n.-17-276G>A
NM_001291970.2:c.138-276G>A (POLH) NP_001278899.1:n.138-276G>A
NM_006502.3:c.138-276G>A (POLH) MANE Select NP_006493.1:n.138-276G>A
NM_001318876.2:c.945+53460G>A (POLR1C) NP_001305805.1:n.945+53460G>A