Canonical Allele Identifier: CA393750566

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89862209C>T (hg19) ; chr15:g.89318978C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318978C>T , CM000677.2:g.89318978C>T	GRCh38
NC_000015.9:g.89862209C>T , CM000677.1:g.89862209C>T	GRCh37
NC_000015.8:g.87663213C>T	NCBI36
NG_008218.1:g.20818G>A
NG_011736.1:g.80016C>T , LRG_500:g.80016C>T
NG_008218.2:g.20818G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3226G>A	ENSP00000516154.1:p.Gly1076Ser
ENST00000268124.11:c.3226G>A MANE Select	ENSP00000268124.5:p.Gly1076Ser
ENST00000530292.3:c.2827G>A	ENSP00000432885.2:p.Gly943Ser
ENST00000635986.2:c.*296G>A	ENSP00000490653.2:n.*296G>A
ENST00000636774.1:c.*1793G>A	ENSP00000489799.1:n.*1793G>A
ENST00000637238.1:c.2035G>A	ENSP00000490756.1:n.2035G>A
ENST00000637264.1:c.2298G>A
ENST00000666746.1:c.2803G>A
ENST00000672071.1:n.3424G>A
ENST00000672695.1:n.403G>A
ENST00000672923.2:n.3226G>A
ENST00000268124.9:c.3226G>A	ENSP00000268124.5:p.Gly1076Ser
ENST00000442287.6:c.3226G>A	ENSP00000399851.2:p.Gly1076Ser
ENST00000530292.2:c.310G>A	ENSP00000432885.1:p.Gly104Ser
ENST00000631044.2:c.*2650G>A	ENSP00000486730.1:n.*2650G>A
NM_001126131.1:c.3226G>A	NP_001119603.1:p.Gly1076Ser
NM_002693.2:c.3226G>A	NP_002684.1:p.Gly1076Ser
NM_001126131.2:c.3226G>A	NP_001119603.1:p.Gly1076Ser
NM_002693.3:c.3226G>A MANE Select	NP_002684.1:p.Gly1076Ser