Canonical Allele Identifier: CA393749913

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89861901C>G (hg19) ; chr15:g.89318670C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318670C>G , CM000677.2:g.89318670C>G	GRCh38
NC_000015.9:g.89861901C>G , CM000677.1:g.89861901C>G	GRCh37
NC_000015.8:g.87662905C>G	NCBI36
NG_008218.1:g.21126G>C
NG_011736.1:g.79708C>G , LRG_500:g.79708C>G
NG_008218.2:g.21126G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3353G>C	ENSP00000516154.1:p.Trp1118Ser
ENST00000268124.11:c.3353G>C MANE Select	ENSP00000268124.5:p.Trp1118Ser
ENST00000530292.3:c.2954G>C	ENSP00000432885.2:p.Trp985Ser
ENST00000635986.2:c.*423G>C	ENSP00000490653.2:n.*423G>C
ENST00000636774.1:c.*1920G>C	ENSP00000489799.1:n.*1920G>C
ENST00000637238.1:c.2162G>C	ENSP00000490756.1:n.2162G>C
ENST00000637264.1:c.2425G>C
ENST00000666746.1:c.2930G>C
ENST00000672071.1:n.3551G>C
ENST00000672695.1:n.530G>C
ENST00000672923.2:n.3353G>C
ENST00000268124.9:c.3353G>C	ENSP00000268124.5:p.Trp1118Ser
ENST00000442287.6:c.3353G>C	ENSP00000399851.2:p.Trp1118Ser
ENST00000530292.2:c.437G>C	ENSP00000432885.1:p.Trp146Ser
ENST00000631044.2:c.*2777G>C	ENSP00000486730.1:n.*2777G>C
NM_001126131.1:c.3353G>C	NP_001119603.1:p.Trp1118Ser
NM_002693.2:c.3353G>C	NP_002684.1:p.Trp1118Ser
NM_001126131.2:c.3353G>C	NP_001119603.1:p.Trp1118Ser
NM_002693.3:c.3353G>C MANE Select	NP_002684.1:p.Trp1118Ser