Canonical Allele Identifier: CA393748183

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89860761C>A (hg19) ; chr15:g.89317530C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89317530C>A , CM000677.2:g.89317530C>A	GRCh38
NC_000015.9:g.89860761C>A , CM000677.1:g.89860761C>A	GRCh37
NC_000015.8:g.87661765C>A	NCBI36
NG_008218.1:g.22266G>T
NG_011736.1:g.78568C>A , LRG_500:g.78568C>A
NG_008218.2:g.22266G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3489G>T	ENSP00000516154.1:p.Met1163Ile
ENST00000268124.11:c.3489G>T MANE Select	ENSP00000268124.5:p.Met1163Ile
ENST00000530292.3:c.3189G>T	ENSP00000432885.2:n.3189G>T
ENST00000635986.2:c.*559G>T	ENSP00000490653.2:n.*559G>T
ENST00000636774.1:c.*2093G>T	ENSP00000489799.1:n.*2093G>T
ENST00000637042.1:n.72-59G>T
ENST00000637238.1:c.2397G>T	ENSP00000490756.1:n.2397G>T
ENST00000637264.1:c.2555-54G>T
ENST00000666746.1:c.3066G>T
ENST00000672071.1:n.4691G>T
ENST00000672695.1:n.1268G>T
ENST00000672923.2:n.3489G>T
ENST00000268124.9:c.3489G>T	ENSP00000268124.5:p.Met1163Ile
ENST00000442287.6:c.3489G>T	ENSP00000399851.2:p.Met1163Ile
ENST00000526671.1:n.299G>T
ENST00000530292.2:c.672G>T	ENSP00000432885.1:n.672G>T
ENST00000631044.2:c.*2913G>T	ENSP00000486730.1:n.*2913G>T
NM_001126131.1:c.3489G>T	NP_001119603.1:p.Met1163Ile
NM_002693.2:c.3489G>T	NP_002684.1:p.Met1163Ile
NM_001126131.2:c.3489G>T	NP_001119603.1:p.Met1163Ile
NM_002693.3:c.3489G>T MANE Select	NP_002684.1:p.Met1163Ile