Canonical Allele Identifier: CA393749741

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89861821C>A (hg19) ; chr15:g.89318590C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318590C>A , CM000677.2:g.89318590C>A	GRCh38
NC_000015.9:g.89861821C>A , CM000677.1:g.89861821C>A	GRCh37
NC_000015.8:g.87662825C>A	NCBI36
NG_008218.1:g.21206G>T
NG_011736.1:g.79628C>A , LRG_500:g.79628C>A
NG_008218.2:g.21206G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3433G>T	ENSP00000516154.1:p.Asp1145Tyr
ENST00000268124.11:c.3433G>T MANE Select	ENSP00000268124.5:p.Asp1145Tyr
ENST00000530292.3:c.3034G>T	ENSP00000432885.2:p.Asp1012Tyr
ENST00000635986.2:c.*503G>T	ENSP00000490653.2:n.*503G>T
ENST00000636774.1:c.*2000G>T	ENSP00000489799.1:n.*2000G>T
ENST00000637238.1:c.2242G>T	ENSP00000490756.1:n.2242G>T
ENST00000637264.1:c.2505G>T
ENST00000666746.1:c.3010G>T
ENST00000672071.1:n.3631G>T
ENST00000672695.1:n.610G>T
ENST00000672923.2:n.3433G>T
ENST00000268124.9:c.3433G>T	ENSP00000268124.5:p.Asp1145Tyr
ENST00000442287.6:c.3433G>T	ENSP00000399851.2:p.Asp1145Tyr
ENST00000530292.2:c.517G>T	ENSP00000432885.1:p.Asp173Tyr
ENST00000631044.2:c.*2857G>T	ENSP00000486730.1:n.*2857G>T
NM_001126131.1:c.3433G>T	NP_001119603.1:p.Asp1145Tyr
NM_002693.2:c.3433G>T	NP_002684.1:p.Asp1145Tyr
NM_001126131.2:c.3433G>T	NP_001119603.1:p.Asp1145Tyr
NM_002693.3:c.3433G>T MANE Select	NP_002684.1:p.Asp1145Tyr