Canonical Allele Identifier: CA2838374094

Gene: POLQ

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121436328_121436335dup , CM000665.2:g.121436328_121436335dup	GRCh38
NC_000003.11:g.121155175_121155182dup , CM000665.1:g.121155175_121155182dup	GRCh37
NC_000003.10:g.122637865_122637872dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264233.6:c.7390-59_7390-52dup MANE Select	ENSP00000264233.5:n.7390-59_7390-52dup
ENST00000264233.5:c.7390-59_7390-52dup	ENSP00000264233.5:n.7390-59_7390-52dup
ENST00000621776.4:c.7795-59_7795-52dup	ENSP00000481120.1:n.7795-59_7795-52dup
NM_199420.3:c.7390-59_7390-52dup	NP_955452.3:n.7390-59_7390-52dup
XM_011512343.1:c.7252-59_7252-52dup	XP_011510645.1:n.7252-59_7252-52dup
XM_011512344.1:c.7003-59_7003-52dup	XP_011510646.1:n.7003-59_7003-52dup
XM_011512345.1:c.6985-59_6985-52dup	XP_011510647.1:n.6985-59_6985-52dup
XM_011512346.1:c.6952-59_6952-52dup	XP_011510648.1:n.6952-59_6952-52dup
XM_011512347.1:c.7390-59_7390-52dup	XP_011510649.1:n.7390-59_7390-52dup
XM_011512348.1:c.6877-59_6877-52dup	XP_011510650.1:n.6877-59_6877-52dup
XM_011512349.1:c.6877-59_6877-52dup	XP_011510651.1:n.6877-59_6877-52dup
XM_011512350.1:c.6598-59_6598-52dup	XP_011510652.1:n.6598-59_6598-52dup
XM_011512351.1:c.6220-59_6220-52dup	XP_011510653.1:n.6220-59_6220-52dup
XM_011512354.1:c.5101-59_5101-52dup	XP_011510656.1:n.5101-59_5101-52dup
XR_924092.1:n.6997-59_6997-52dup
XM_011512343.2:c.7252-59_7252-52dup	XP_011510645.1:n.7252-59_7252-52dup
XM_011512347.2:c.7390-59_7390-52dup	XP_011510649.1:n.7390-59_7390-52dup
XM_011512348.2:c.6877-59_6877-52dup	XP_011510650.1:n.6877-59_6877-52dup
XM_011512354.2:c.5101-59_5101-52dup	XP_011510656.1:n.5101-59_5101-52dup
XM_017005565.1:c.6220-59_6220-52dup	XP_016861054.1:n.6220-59_6220-52dup
XR_001739986.1:n.7009-59_7009-52dup
NM_199420.4:c.7390-59_7390-52dup MANE Select	NP_955452.3:n.7390-59_7390-52dup