Canonical Allele Identifier: CA393751185

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89862316T>A (hg19) ; chr15:g.89319085T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89319085T>A , CM000677.2:g.89319085T>A	GRCh38
NC_000015.9:g.89862316T>A , CM000677.1:g.89862316T>A	GRCh37
NC_000015.8:g.87663320T>A	NCBI36
NG_008218.1:g.20711A>T
NG_011736.1:g.80123T>A , LRG_500:g.80123T>A
NG_008218.2:g.20711A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3119A>T	ENSP00000516154.1:p.Lys1040Met
ENST00000268124.11:c.3119A>T MANE Select	ENSP00000268124.5:p.Lys1040Met
ENST00000530292.3:c.2720A>T	ENSP00000432885.2:p.Lys907Met
ENST00000635986.2:c.*189A>T	ENSP00000490653.2:n.*189A>T
ENST00000636530.1:n.79A>T
ENST00000636774.1:c.*1686A>T	ENSP00000489799.1:n.*1686A>T
ENST00000637238.1:c.1928A>T	ENSP00000490756.1:n.1928A>T
ENST00000637264.1:c.2191A>T
ENST00000666746.1:c.2696A>T
ENST00000672071.1:n.3317A>T
ENST00000672695.1:n.296A>T
ENST00000672923.2:n.3119A>T
ENST00000268124.9:c.3119A>T	ENSP00000268124.5:p.Lys1040Met
ENST00000442287.6:c.3119A>T	ENSP00000399851.2:p.Lys1040Met
ENST00000530292.2:c.203A>T	ENSP00000432885.1:p.Lys68Met
ENST00000631044.2:c.*2543A>T	ENSP00000486730.1:n.*2543A>T
NM_001126131.1:c.3119A>T	NP_001119603.1:p.Lys1040Met
NM_002693.2:c.3119A>T	NP_002684.1:p.Lys1040Met
NM_001126131.2:c.3119A>T	NP_001119603.1:p.Lys1040Met
NM_002693.3:c.3119A>T MANE Select	NP_002684.1:p.Lys1040Met