Canonical Allele Identifier: CA393749948

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89861918C>T (hg19) ; chr15:g.89318687C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318687C>T , CM000677.2:g.89318687C>T	GRCh38
NC_000015.9:g.89861918C>T , CM000677.1:g.89861918C>T	GRCh37
NC_000015.8:g.87662922C>T	NCBI36
NG_008218.1:g.21109G>A
NG_011736.1:g.79725C>T , LRG_500:g.79725C>T
NG_008218.2:g.21109G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3336G>A	ENSP00000516154.1:p.Met1112Ile
ENST00000268124.11:c.3336G>A MANE Select	ENSP00000268124.5:p.Met1112Ile
ENST00000530292.3:c.2937G>A	ENSP00000432885.2:p.Met979Ile
ENST00000635986.2:c.*406G>A	ENSP00000490653.2:n.*406G>A
ENST00000636774.1:c.*1903G>A	ENSP00000489799.1:n.*1903G>A
ENST00000637238.1:c.2145G>A	ENSP00000490756.1:n.2145G>A
ENST00000637264.1:c.2408G>A
ENST00000666746.1:c.2913G>A
ENST00000672071.1:n.3534G>A
ENST00000672695.1:n.513G>A
ENST00000672923.2:n.3336G>A
ENST00000268124.9:c.3336G>A	ENSP00000268124.5:p.Met1112Ile
ENST00000442287.6:c.3336G>A	ENSP00000399851.2:p.Met1112Ile
ENST00000530292.2:c.420G>A	ENSP00000432885.1:p.Met140Ile
ENST00000631044.2:c.*2760G>A	ENSP00000486730.1:n.*2760G>A
NM_001126131.1:c.3336G>A	NP_001119603.1:p.Met1112Ile
NM_002693.2:c.3336G>A	NP_002684.1:p.Met1112Ile
NM_001126131.2:c.3336G>A	NP_001119603.1:p.Met1112Ile
NM_002693.3:c.3336G>A MANE Select	NP_002684.1:p.Met1112Ile