Canonical Allele Identifier: CA1624610408

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43587326T= , CM000668.2:g.43587326T= GRCh38
NC_000006.11:g.43555063T= , CM000668.1:g.43555063T= GRCh37
NC_000006.10:g.43663041T= NCBI36
NG_009252.1:g.16186T= , LRG_470:g.16186T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372236.9:c.327T= (POLH) MANE Select ENSP00000361310.4:p.Ile109=
ENST00000372226.1:c.327T= (POLH) ENSP00000361300.1:p.Ile109=
ENST00000372236.8:c.327T= (POLH) ENSP00000361310.4:p.Ile109=
ENST00000443535.1:c.141T= (POLH) ENSP00000405320.1:p.Ile47=
NM_001291969.1:c.118+4185T= (POLH) NP_001278898.1:n.118+4185T=
NM_001291970.1:c.327T= (POLH) NP_001278899.1:p.Ile109=
NM_006502.2:c.327T= , LRG_470t1:c.327T= (POLH) NP_006493.1:p.Ile109=
XM_005249186.2:c.141T= (POLH) XP_005249243.1:p.Ile47=
XM_011514698.1:c.118+4185T= (POLH) XP_011513000.1:n.118+4185T=
XM_005249186.4:c.141T= (POLH) XP_005249243.1:p.Ile47=
XM_011514698.3:c.118+4185T= (POLH) XP_011513000.1:n.118+4185T=
XM_024446466.1:c.75T= (POLH) XP_024302234.1:p.Ile25=
XM_024446467.1:c.-293T= (POLH) XP_024302235.1:n.-293T=
NM_001291969.2:c.118+4185T= (POLH) NP_001278898.1:n.118+4185T=
NM_001291970.2:c.327T= (POLH) NP_001278899.1:p.Ile109=
NM_006502.3:c.327T= (POLH) MANE Select NP_006493.1:p.Ile109=
NM_001318876.2:c.945+58055T= (POLR1C) NP_001305805.1:n.945+58055T=