Canonical Allele Identifier: CA1624610400

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43587308G= , CM000668.2:g.43587308G= GRCh38
NC_000006.11:g.43555045G= , CM000668.1:g.43555045G= GRCh37
NC_000006.10:g.43663023G= NCBI36
NG_009252.1:g.16168G= , LRG_470:g.16168G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372236.9:c.309G= (POLH) MANE Select ENSP00000361310.4:p.Met103=
ENST00000372226.1:c.309G= (POLH) ENSP00000361300.1:p.Met103=
ENST00000372236.8:c.309G= (POLH) ENSP00000361310.4:p.Met103=
ENST00000443535.1:c.123G= (POLH) ENSP00000405320.1:p.Met41=
NM_001291969.1:c.118+4167G= (POLH) NP_001278898.1:n.118+4167G=
NM_001291970.1:c.309G= (POLH) NP_001278899.1:p.Met103=
NM_006502.2:c.309G= , LRG_470t1:c.309G= (POLH) NP_006493.1:p.Met103=
XM_005249186.2:c.123G= (POLH) XP_005249243.1:p.Met41=
XM_011514698.1:c.118+4167G= (POLH) XP_011513000.1:n.118+4167G=
XM_005249186.4:c.123G= (POLH) XP_005249243.1:p.Met41=
XM_011514698.3:c.118+4167G= (POLH) XP_011513000.1:n.118+4167G=
XM_024446466.1:c.57G= (POLH) XP_024302234.1:p.Met19=
XM_024446467.1:c.-311G= (POLH) XP_024302235.1:n.-311G=
NM_001291969.2:c.118+4167G= (POLH) NP_001278898.1:n.118+4167G=
NM_001291970.2:c.309G= (POLH) NP_001278899.1:p.Met103=
NM_006502.3:c.309G= (POLH) MANE Select NP_006493.1:p.Met103=
NM_001318876.2:c.945+58037G= (POLR1C) NP_001305805.1:n.945+58037G=