Canonical Allele Identifier: CA1624610392

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43587276_43587277delinsCG , CM000668.2:g.43587276_43587277delinsCG GRCh38
NC_000006.11:g.43555013_43555014delinsCG , CM000668.1:g.43555013_43555014delinsCG GRCh37
NC_000006.10:g.43662991_43662992delinsCG NCBI36
NG_009252.1:g.16136_16137delinsCG , LRG_470:g.16136_16137delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000372236.9:c.277_278delinsCG (POLH) MANE Select ENSP00000361310.4:p.Arg93=
ENST00000372226.1:c.277_278delinsCG (POLH) ENSP00000361300.1:p.Arg93=
ENST00000372236.8:c.277_278delinsCG (POLH) ENSP00000361310.4:p.Arg93=
ENST00000443535.1:c.91_92delinsCG (POLH) ENSP00000405320.1:p.Arg31=
NM_001291969.1:c.118+4135_118+4136delinsCG (POLH) NP_001278898.1:n.118+4135_118+4136delinsCG
NM_001291970.1:c.277_278delinsCG (POLH) NP_001278899.1:p.Arg93=
NM_006502.2:c.277_278delinsCG , LRG_470t1:c.277_278delinsCG (POLH) NP_006493.1:p.Arg93=
XM_005249186.2:c.91_92delinsCG (POLH) XP_005249243.1:p.Arg31=
XM_011514698.1:c.118+4135_118+4136delinsCG (POLH) XP_011513000.1:n.118+4135_118+4136delinsCG
XM_005249186.4:c.91_92delinsCG (POLH) XP_005249243.1:p.Arg31=
XM_011514698.3:c.118+4135_118+4136delinsCG (POLH) XP_011513000.1:n.118+4135_118+4136delinsCG
XM_024446466.1:c.25_26delinsCG (POLH) XP_024302234.1:p.Arg9=
XM_024446467.1:c.-343_-342delinsCG (POLH) XP_024302235.1:n.-343_-342delinsCG
NM_001291969.2:c.118+4135_118+4136delinsCG (POLH) NP_001278898.1:n.118+4135_118+4136delinsCG
NM_001291970.2:c.277_278delinsCG (POLH) NP_001278899.1:p.Arg93=
NM_006502.3:c.277_278delinsCG (POLH) MANE Select NP_006493.1:p.Arg93=
NM_001318876.2:c.945+58005_945+58006delinsCG (POLR1C) NP_001305805.1:n.945+58005_945+58006delinsCG