Canonical Allele Identifier: CA393766941

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89873397G>A (hg19) ; chr15:g.89330166G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89330166G>A , CM000677.2:g.89330166G>A	GRCh38
NC_000015.9:g.89873397G>A , CM000677.1:g.89873397G>A	GRCh37
NC_000015.8:g.87674401G>A	NCBI36
NG_008218.1:g.9630C>T
NG_008218.2:g.9630C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.770C>T	ENSP00000516154.1:p.Thr257Ile
ENST00000268124.11:c.770C>T MANE Select	ENSP00000268124.5:p.Thr257Ile
ENST00000530292.3:c.371C>T	ENSP00000432885.2:p.Thr124Ile
ENST00000635986.2:c.770C>T	ENSP00000490653.2:p.Thr257Ile
ENST00000636774.1:c.770C>T	ENSP00000489799.1:p.Thr257Ile
ENST00000666746.1:c.427C>T
ENST00000672071.1:n.968C>T
ENST00000268124.9:c.770C>T	ENSP00000268124.5:p.Thr257Ile
ENST00000442287.6:c.770C>T	ENSP00000399851.2:p.Thr257Ile
ENST00000631044.2:c.*153C>T	ENSP00000486730.1:n.*153C>T
NM_001126131.1:c.770C>T	NP_001119603.1:p.Thr257Ile
NM_002693.2:c.770C>T	NP_002684.1:p.Thr257Ile
NM_001126131.2:c.770C>T	NP_001119603.1:p.Thr257Ile
NM_002693.3:c.770C>T MANE Select	NP_002684.1:p.Thr257Ile