Canonical Allele Identifier: CA393749939

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89861913A>G (hg19) ; chr15:g.89318682A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318682A>G , CM000677.2:g.89318682A>G	GRCh38
NC_000015.9:g.89861913A>G , CM000677.1:g.89861913A>G	GRCh37
NC_000015.8:g.87662917A>G	NCBI36
NG_008218.1:g.21114T>C
NG_011736.1:g.79720A>G , LRG_500:g.79720A>G
NG_008218.2:g.21114T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3341T>C	ENSP00000516154.1:p.Val1114Ala
ENST00000268124.11:c.3341T>C MANE Select	ENSP00000268124.5:p.Val1114Ala
ENST00000530292.3:c.2942T>C	ENSP00000432885.2:p.Val981Ala
ENST00000635986.2:c.*411T>C	ENSP00000490653.2:n.*411T>C
ENST00000636774.1:c.*1908T>C	ENSP00000489799.1:n.*1908T>C
ENST00000637238.1:c.2150T>C	ENSP00000490756.1:n.2150T>C
ENST00000637264.1:c.2413T>C
ENST00000666746.1:c.2918T>C
ENST00000672071.1:n.3539T>C
ENST00000672695.1:n.518T>C
ENST00000672923.2:n.3341T>C
ENST00000268124.9:c.3341T>C	ENSP00000268124.5:p.Val1114Ala
ENST00000442287.6:c.3341T>C	ENSP00000399851.2:p.Val1114Ala
ENST00000530292.2:c.425T>C	ENSP00000432885.1:p.Val142Ala
ENST00000631044.2:c.*2765T>C	ENSP00000486730.1:n.*2765T>C
NM_001126131.1:c.3341T>C	NP_001119603.1:p.Val1114Ala
NM_002693.2:c.3341T>C	NP_002684.1:p.Val1114Ala
NM_001126131.2:c.3341T>C	NP_001119603.1:p.Val1114Ala
NM_002693.3:c.3341T>C MANE Select	NP_002684.1:p.Val1114Ala