Canonical Allele Identifier: CA1624610412

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43587330C= , CM000668.2:g.43587330C= GRCh38
NC_000006.11:g.43555067C= , CM000668.1:g.43555067C= GRCh37
NC_000006.10:g.43663045C= NCBI36
NG_009252.1:g.16190C= , LRG_470:g.16190C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372236.9:c.331C= (POLH) MANE Select ENSP00000361310.4:p.Arg111=
ENST00000372226.1:c.331C= (POLH) ENSP00000361300.1:p.Arg111=
ENST00000372236.8:c.331C= (POLH) ENSP00000361310.4:p.Arg111=
ENST00000443535.1:c.145C= (POLH) ENSP00000405320.1:p.Arg49=
NM_001291969.1:c.118+4189C= (POLH) NP_001278898.1:n.118+4189C=
NM_001291970.1:c.331C= (POLH) NP_001278899.1:p.Arg111=
NM_006502.2:c.331C= , LRG_470t1:c.331C= (POLH) NP_006493.1:p.Arg111=
XM_005249186.2:c.145C= (POLH) XP_005249243.1:p.Arg49=
XM_011514698.1:c.118+4189C= (POLH) XP_011513000.1:n.118+4189C=
XM_005249186.4:c.145C= (POLH) XP_005249243.1:p.Arg49=
XM_011514698.3:c.118+4189C= (POLH) XP_011513000.1:n.118+4189C=
XM_024446466.1:c.79C= (POLH) XP_024302234.1:p.Arg27=
XM_024446467.1:c.-289C= (POLH) XP_024302235.1:n.-289C=
NM_001291969.2:c.118+4189C= (POLH) NP_001278898.1:n.118+4189C=
NM_001291970.2:c.331C= (POLH) NP_001278899.1:p.Arg111=
NM_006502.3:c.331C= (POLH) MANE Select NP_006493.1:p.Arg111=
NM_001318876.2:c.945+58059C= (POLR1C) NP_001305805.1:n.945+58059C=