Canonical Allele Identifier: CA393748211

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89860764G>T (hg19) ; chr15:g.89317533G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89317533G>T , CM000677.2:g.89317533G>T	GRCh38
NC_000015.9:g.89860764G>T , CM000677.1:g.89860764G>T	GRCh37
NC_000015.8:g.87661768G>T	NCBI36
NG_008218.1:g.22263C>A
NG_011736.1:g.78571G>T , LRG_500:g.78571G>T
NG_008218.2:g.22263C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3486C>A	ENSP00000516154.1:p.Cys1162Ter
ENST00000268124.11:c.3486C>A MANE Select	ENSP00000268124.5:p.Cys1162Ter
ENST00000530292.3:c.3186C>A	ENSP00000432885.2:n.3186C>A
ENST00000635986.2:c.*556C>A	ENSP00000490653.2:n.*556C>A
ENST00000636774.1:c.*2090C>A	ENSP00000489799.1:n.*2090C>A
ENST00000637042.1:n.72-62C>A
ENST00000637238.1:c.2394C>A	ENSP00000490756.1:n.2394C>A
ENST00000637264.1:c.2555-57C>A
ENST00000666746.1:c.3063C>A
ENST00000672071.1:n.4688C>A
ENST00000672695.1:n.1265C>A
ENST00000672923.2:n.3486C>A
ENST00000268124.9:c.3486C>A	ENSP00000268124.5:p.Cys1162Ter
ENST00000442287.6:c.3486C>A	ENSP00000399851.2:p.Cys1162Ter
ENST00000526671.1:n.296C>A
ENST00000530292.2:c.669C>A	ENSP00000432885.1:n.669C>A
ENST00000631044.2:c.*2910C>A	ENSP00000486730.1:n.*2910C>A
NM_001126131.1:c.3486C>A	NP_001119603.1:p.Cys1162Ter
NM_002693.2:c.3486C>A	NP_002684.1:p.Cys1162Ter
NM_001126131.2:c.3486C>A	NP_001119603.1:p.Cys1162Ter
NM_002693.3:c.3486C>A MANE Select	NP_002684.1:p.Cys1162Ter