Canonical Allele Identifier: CA1979153795

Gene: POLA2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65297219G= , CM000673.2:g.65297219G=	GRCh38
NC_000011.9:g.65064690G= , CM000673.1:g.65064690G=	GRCh37
NC_000011.8:g.64821266G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002689.4:c.1747G= MANE Select	NP_002680.2:p.Gly583=
ENST00000265465.8:c.1747G= MANE Select	ENSP00000265465.3:p.Gly583=
NM_002689.3:c.1747G=	NP_002680.2:p.Gly583=
ENST00000265465.7:c.1747G=	ENSP00000265465.3:p.Gly583=
ENST00000525924.1:c.656+1229G=
ENST00000525924.2:c.1647+1229G=	ENSP00000434173.2:n.1647+1229G=
ENST00000527618.5:n.1527G=
ENST00000527618.6:n.3473G=
ENST00000534785.1:n.408G=
ENST00000649896.1:c.1647+1229G=	ENSP00000498025.1:n.1647+1229G=
ENST00000706534.1:c.*1602G=	ENSP00000516436.1:n.*1602G=
ENST00000706535.1:c.*1508G=	ENSP00000516437.1:n.*1508G=
ENST00000706537.1:c.*101G=	ENSP00000516439.1:n.*101G=
ENST00000706538.1:c.*114G=	ENSP00000516440.1:n.*114G=
ENST00000706540.1:c.*979+1229G=	ENSP00000516441.1:n.*979+1229G=
ENST00000706541.1:n.2936G=
XM_011544877.1:c.1647+1229G=	XP_011543179.1:n.1647+1229G=
XM_011544877.3:c.1647+1229G=	XP_011543179.1:n.1647+1229G=
XM_011544878.1:c.1647+1229G=	XP_011543180.1:n.1647+1229G=
XM_011544878.3:c.1647+1229G=	XP_011543180.1:n.1647+1229G=
XM_011544879.1:c.*114G=	XP_011543181.1:n.*114G=
XM_011544879.2:c.*114G=	XP_011543181.1:n.*114G=
XM_011544880.1:c.*14+1229G=	XP_011543182.1:n.*14+1229G=
XM_011544881.1:c.*15-453G=	XP_011543183.1:n.*15-453G=
XM_011544881.3:c.*15-453G=	XP_011543183.1:n.*15-453G=
XM_017017452.2:c.1648-453G=	XP_016872941.1:n.1648-453G=