Canonical Allele Identifier: CA16607917

Gene: POLG

Linked Data

• ClinVar Variation Id: 385287
• ClinVar RCV Id: RCV000425327
• dbSNP Id: rs1057522174
• MyVariant Identifiers: chr15:g.89870384C>G (hg19) ; chr15:g.89327153C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89327153C>G , CM000677.2:g.89327153C>G	GRCh38
NC_000015.9:g.89870384C>G , CM000677.1:g.89870384C>G	GRCh37
NC_000015.8:g.87671388C>G	NCBI36
NG_008218.1:g.12643G>C
NG_008218.2:g.12643G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.1433+14G>C	ENSP00000516154.1:n.1433+14G>C
ENST00000268124.11:c.1433+14G>C MANE Select	ENSP00000268124.5:n.1433+14G>C
ENST00000530292.3:c.1034+14G>C	ENSP00000432885.2:n.1034+14G>C
ENST00000635986.2:c.1433+14G>C	ENSP00000490653.2:n.1433+14G>C
ENST00000636774.1:c.1433+14G>C	ENSP00000489799.1:n.1433+14G>C
ENST00000637238.1:c.170+14G>C	ENSP00000490756.1:n.170+14G>C
ENST00000637264.1:c.505+14G>C
ENST00000666746.1:c.1010+14G>C
ENST00000672071.1:n.1631+14G>C
ENST00000672923.2:n.1536+14G>C
ENST00000268124.9:c.1433+14G>C	ENSP00000268124.5:n.1433+14G>C
ENST00000442287.6:c.1433+14G>C	ENSP00000399851.2:n.1433+14G>C
ENST00000532363.2:n.305G>C
ENST00000631044.2:c.*816+14G>C	ENSP00000486730.1:n.*816+14G>C
NM_001126131.1:c.1433+14G>C	NP_001119603.1:n.1433+14G>C
NM_002693.2:c.1433+14G>C	NP_002684.1:n.1433+14G>C
NM_001126131.2:c.1433+14G>C	NP_001119603.1:n.1433+14G>C
NM_002693.3:c.1433+14G>C MANE Select	NP_002684.1:n.1433+14G>C