Canonical Allele Identifier: CA3827253

Gene: POLH GTPBP2 POLR1C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43613888G>A , CM000668.2:g.43613888G>A	GRCh38
NC_000006.11:g.43581625G>A , CM000668.1:g.43581625G>A	GRCh37
NC_000006.10:g.43689603G>A	NCBI36
NG_009252.1:g.42748G>A , LRG_470:g.42748G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006502.3:c.1473G>A (POLH) MANE Select	NP_006493.1:p.Gln491=
ENST00000372236.9:c.1473G>A (POLH) MANE Select	ENSP00000361310.4:p.Gln491=
NM_001291969.1:c.1101G>A (POLH)	NP_001278898.1:p.Gln367=
NM_001291969.2:c.1101G>A (POLH)	NP_001278898.1:p.Gln367=
NM_001291970.1:c.*157G>A (POLH)	NP_001278899.1:n.*157G>A
NM_001291970.2:c.*157G>A (POLH)	NP_001278899.1:n.*157G>A
NM_001318876.2:c.945+84617G>A (POLR1C)	NP_001305805.1:n.945+84617G>A
NM_006502.2:c.1473G>A , LRG_470t1:c.1473G>A (POLH)	NP_006493.1:p.Gln491=
ENST00000372226.1:c.*157G>A (POLH)	ENSP00000361300.1:n.*157G>A
ENST00000372236.8:c.1473G>A (POLH)	ENSP00000361310.4:p.Gln491=
ENST00000496137.5:c.449+6231C>T (GTPBP2)	ENSP00000436973.1:n.449+6231C>T
XM_005249186.2:c.1287G>A (POLH)	XP_005249243.1:p.Gln429=
XM_005249186.4:c.1287G>A (POLH)	XP_005249243.1:p.Gln429=
XM_011514698.1:c.1101G>A (POLH)	XP_011513000.1:p.Gln367=
XM_011514698.3:c.1101G>A (POLH)	XP_011513000.1:p.Gln367=
XM_024446466.1:c.1221G>A (POLH)	XP_024302234.1:p.Gln407=
XM_024446467.1:c.1017G>A (POLH)	XP_024302235.1:p.Gln339=