Canonical Allele Identifier: CA393753022

Gene: POLG

Linked Data

• gnomAD v4: 15-89320940-G-A
• MyVariant Identifiers: chr15:g.89864171G>A (hg19) ; chr15:g.89320940G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89320940G>A , CM000677.2:g.89320940G>A	GRCh38
NC_000015.9:g.89864171G>A , CM000677.1:g.89864171G>A	GRCh37
NC_000015.8:g.87665175G>A	NCBI36
NG_008218.1:g.18856C>T
NG_008218.2:g.18856C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2807C>T	ENSP00000516154.1:p.Ala936Val
ENST00000268124.11:c.2807C>T MANE Select	ENSP00000268124.5:p.Ala936Val
ENST00000530292.3:c.2408C>T	ENSP00000432885.2:p.Ala803Val
ENST00000635986.2:c.2807C>T	ENSP00000490653.2:p.Ala936Val
ENST00000636774.1:c.*1374C>T	ENSP00000489799.1:n.*1374C>T
ENST00000637238.1:c.1616C>T	ENSP00000490756.1:n.1616C>T
ENST00000637264.1:c.1879C>T
ENST00000666746.1:c.2384C>T
ENST00000670281.1:c.800+1022C>T	ENSP00000499709.1:n.800+1022C>T
ENST00000672071.1:n.3005C>T
ENST00000672923.2:n.2749C>T
ENST00000268124.9:c.2807C>T	ENSP00000268124.5:p.Ala936Val
ENST00000442287.6:c.2807C>T	ENSP00000399851.2:p.Ala936Val
ENST00000528881.2:c.404C>T
ENST00000530715.5:c.186-71C>T	ENSP00000431395.1:n.186-71C>T
ENST00000631044.2:c.*2231C>T	ENSP00000486730.1:n.*2231C>T
NM_001126131.1:c.2807C>T	NP_001119603.1:p.Ala936Val
NM_002693.2:c.2807C>T	NP_002684.1:p.Ala936Val
NM_001126131.2:c.2807C>T	NP_001119603.1:p.Ala936Val
NM_002693.3:c.2807C>T MANE Select	NP_002684.1:p.Ala936Val