Canonical Allele Identifier: CA1624576271

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43587450C= , CM000668.2:g.43587450C= GRCh38
NC_000006.11:g.43555187C= , CM000668.1:g.43555187C= GRCh37
NC_000006.10:g.43663165C= NCBI36
NG_009252.1:g.16310C= , LRG_470:g.16310C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372236.9:c.451C= (POLH) MANE Select ENSP00000361310.4:p.Pro151=
ENST00000372226.1:c.451C= (POLH) ENSP00000361300.1:p.Pro151=
ENST00000372236.8:c.451C= (POLH) ENSP00000361310.4:p.Pro151=
NM_001291969.1:c.118+4309C= (POLH) NP_001278898.1:n.118+4309C=
NM_001291970.1:c.451C= (POLH) NP_001278899.1:p.Pro151=
NM_006502.2:c.451C= , LRG_470t1:c.451C= (POLH) NP_006493.1:p.Pro151=
XM_005249186.2:c.265C= (POLH) XP_005249243.1:p.Pro89=
XM_011514698.1:c.118+4309C= (POLH) XP_011513000.1:n.118+4309C=
XM_005249186.4:c.265C= (POLH) XP_005249243.1:p.Pro89=
XM_011514698.3:c.118+4309C= (POLH) XP_011513000.1:n.118+4309C=
XM_024446466.1:c.199C= (POLH) XP_024302234.1:p.Pro67=
XM_024446467.1:c.-169C= (POLH) XP_024302235.1:n.-169C=
NM_001291969.2:c.118+4309C= (POLH) NP_001278898.1:n.118+4309C=
NM_001291970.2:c.451C= (POLH) NP_001278899.1:p.Pro151=
NM_006502.3:c.451C= (POLH) MANE Select NP_006493.1:p.Pro151=
NM_001318876.2:c.945+58179C= (POLR1C) NP_001305805.1:n.945+58179C=