Canonical Allele Identifier: CA2194566120

Gene: POLG POLGARF

Linked Data

• dbSNP Id: rs1596360511

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89330408T>G , CM000677.2:g.89330408T>G	GRCh38
NC_000015.9:g.89873639T>G , CM000677.1:g.89873639T>G	GRCh37
NC_000015.8:g.87674643T>G	NCBI36
NG_008218.1:g.9388A>C
NG_008218.2:g.9388A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.660-132A>C (POLG)	ENSP00000516154.1:n.660-132A>C
ENST00000706918.1:c.715-132A>C (POLGARF)	ENSP00000516626.1:n.715-132A>C
ENST00000268124.11:c.660-132A>C (POLG) MANE Select	ENSP00000268124.5:n.660-132A>C
ENST00000530292.3:c.261-132A>C (POLG)	ENSP00000432885.2:n.261-132A>C
ENST00000635986.2:c.660-132A>C (POLG)	ENSP00000490653.2:n.660-132A>C
ENST00000636774.1:c.660-132A>C (POLG)	ENSP00000489799.1:n.660-132A>C
ENST00000637307.1:c.50-147A>C (POLG)
ENST00000650303.2:c.715-132A>C (POLG)	ENSP00000497242.2:n.715-132A>C
ENST00000666746.1:c.317-132A>C (POLG)
ENST00000672071.1:n.858-132A>C (POLG)
ENST00000268124.9:c.660-132A>C (POLG)	ENSP00000268124.5:n.660-132A>C
ENST00000442287.6:c.660-132A>C (POLG)	ENSP00000399851.2:n.660-132A>C
ENST00000631044.2:c.*43-132A>C (POLG)	ENSP00000486730.1:n.*43-132A>C
NM_001126131.1:c.660-132A>C (POLG)	NP_001119603.1:n.660-132A>C
NM_002693.2:c.660-132A>C (POLG)	NP_002684.1:n.660-132A>C
NM_001126131.2:c.660-132A>C (POLG)	NP_001119603.1:n.660-132A>C
NM_002693.3:c.660-132A>C (POLG) MANE Select	NP_002684.1:n.660-132A>C