Canonical Allele Identifier: CA492071444

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89861792C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318561C>T , CM000677.2:g.89318561C>T	GRCh38
NC_000015.9:g.89861792C>T , CM000677.1:g.89861792C>T	GRCh37
NC_000015.8:g.87662796C>T	NCBI36
NG_008218.1:g.21235G>A
NG_011736.1:g.79599C>T , LRG_500:g.79599C>T
NG_008218.2:g.21235G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3462G>A	ENSP00000516154.1:p.Gln1154=
ENST00000268124.11:c.3462G>A MANE Select	ENSP00000268124.5:p.Gln1154=
ENST00000530292.3:c.3063G>A	ENSP00000432885.2:p.Gln1021=
ENST00000635986.2:c.*532G>A	ENSP00000490653.2:n.*532G>A
ENST00000636774.1:c.*2029G>A	ENSP00000489799.1:n.*2029G>A
ENST00000637238.1:c.2271G>A	ENSP00000490756.1:n.2271G>A
ENST00000637264.1:c.2534G>A
ENST00000666746.1:c.3039G>A
ENST00000672071.1:n.3660G>A
ENST00000672695.1:n.639G>A
ENST00000672923.2:n.3462G>A
ENST00000268124.9:c.3462G>A	ENSP00000268124.5:p.Gln1154=
ENST00000442287.6:c.3462G>A	ENSP00000399851.2:p.Gln1154=
ENST00000530292.2:c.546G>A	ENSP00000432885.1:p.Gln182=
ENST00000631044.2:c.*2886G>A	ENSP00000486730.1:n.*2886G>A
NM_001126131.1:c.3462G>A	NP_001119603.1:p.Gln1154=
NM_002693.2:c.3462G>A	NP_002684.1:p.Gln1154=
NM_001126131.2:c.3462G>A	NP_001119603.1:p.Gln1154=
NM_002693.3:c.3462G>A MANE Select	NP_002684.1:p.Gln1154=