Canonical Allele Identifier: CA393762089

Gene: POLG

Linked Data

• ClinVar Variation Id: 2677961
• ClinVar RCV Id: RCV003471718
• gnomAD v4: 15-89327244-A-C
• MyVariant Identifiers: chr15:g.89870475A>C (hg19) ; chr15:g.89327244A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89327244A>C , CM000677.2:g.89327244A>C	GRCh38
NC_000015.9:g.89870475A>C , CM000677.1:g.89870475A>C	GRCh37
NC_000015.8:g.87671479A>C	NCBI36
NG_008218.1:g.12552T>G
NG_008218.2:g.12552T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1356T>G	ENSP00000516154.1:p.Tyr452Ter
ENST00000268124.11:c.1356T>G MANE Select	ENSP00000268124.5:p.Tyr452Ter
ENST00000530292.3:c.957T>G	ENSP00000432885.2:p.Tyr319Ter
ENST00000635986.2:c.1356T>G	ENSP00000490653.2:p.Tyr452Ter
ENST00000636774.1:c.1356T>G	ENSP00000489799.1:p.Tyr452Ter
ENST00000637238.1:c.93T>G	ENSP00000490756.1:p.Tyr31Ter
ENST00000637264.1:c.428T>G
ENST00000666746.1:c.933T>G
ENST00000672071.1:n.1554T>G
ENST00000672923.2:n.1459T>G
ENST00000268124.9:c.1356T>G	ENSP00000268124.5:p.Tyr452Ter
ENST00000442287.6:c.1356T>G	ENSP00000399851.2:p.Tyr452Ter
ENST00000532363.2:n.214T>G
ENST00000631044.2:c.*739T>G	ENSP00000486730.1:n.*739T>G
NM_001126131.1:c.1356T>G	NP_001119603.1:p.Tyr452Ter
NM_002693.2:c.1356T>G	NP_002684.1:p.Tyr452Ter
NM_001126131.2:c.1356T>G	NP_001119603.1:p.Tyr452Ter
NM_002693.3:c.1356T>G MANE Select	NP_002684.1:p.Tyr452Ter