Canonical Allele Identifier: CA2575828931

Gene: POLG

Linked Data

• gnomAD v4: 15-89329982-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89329982G>C , CM000677.2:g.89329982G>C	GRCh38
NC_000015.9:g.89873213G>C , CM000677.1:g.89873213G>C	GRCh37
NC_000015.8:g.87674217G>C	NCBI36
NG_008218.1:g.9814C>G
NG_008218.2:g.9814C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.855+99C>G	ENSP00000516154.1:n.855+99C>G
ENST00000268124.11:c.855+99C>G MANE Select	ENSP00000268124.5:n.855+99C>G
ENST00000530292.3:c.456+99C>G	ENSP00000432885.2:n.456+99C>G
ENST00000635986.2:c.855+99C>G	ENSP00000490653.2:n.855+99C>G
ENST00000636774.1:c.855+99C>G	ENSP00000489799.1:n.855+99C>G
ENST00000666746.1:c.512+99C>G
ENST00000672071.1:n.1053+99C>G
ENST00000268124.9:c.855+99C>G	ENSP00000268124.5:n.855+99C>G
ENST00000442287.6:c.855+99C>G	ENSP00000399851.2:n.855+99C>G
ENST00000631044.2:c.*238+99C>G	ENSP00000486730.1:n.*238+99C>G
NM_001126131.1:c.855+99C>G	NP_001119603.1:n.855+99C>G
NM_002693.2:c.855+99C>G	NP_002684.1:n.855+99C>G
NM_001126131.2:c.855+99C>G	NP_001119603.1:n.855+99C>G
NM_002693.3:c.855+99C>G MANE Select	NP_002684.1:n.855+99C>G