Canonical Allele Identifier: CA393767043

Gene: POLG

Linked Data

• ClinVar Variation Id: 2869186
• ClinVar RCV Id: RCV003626360
• MyVariant Identifiers: chr15:g.89873437G>A (hg19) ; chr15:g.89330206G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89330206G>A , CM000677.2:g.89330206G>A	GRCh38
NC_000015.9:g.89873437G>A , CM000677.1:g.89873437G>A	GRCh37
NC_000015.8:g.87674441G>A	NCBI36
NG_008218.1:g.9590C>T
NG_008218.2:g.9590C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.730C>T	ENSP00000516154.1:p.Leu244Phe
ENST00000268124.11:c.730C>T MANE Select	ENSP00000268124.5:p.Leu244Phe
ENST00000530292.3:c.331C>T	ENSP00000432885.2:p.Leu111Phe
ENST00000635986.2:c.730C>T	ENSP00000490653.2:p.Leu244Phe
ENST00000636774.1:c.730C>T	ENSP00000489799.1:p.Leu244Phe
ENST00000666746.1:c.387C>T
ENST00000672071.1:n.928C>T
ENST00000268124.9:c.730C>T	ENSP00000268124.5:p.Leu244Phe
ENST00000442287.6:c.730C>T	ENSP00000399851.2:p.Leu244Phe
ENST00000631044.2:c.*113C>T	ENSP00000486730.1:n.*113C>T
NM_001126131.1:c.730C>T	NP_001119603.1:p.Leu244Phe
NM_002693.2:c.730C>T	NP_002684.1:p.Leu244Phe
NM_001126131.2:c.730C>T	NP_001119603.1:p.Leu244Phe
NM_002693.3:c.730C>T MANE Select	NP_002684.1:p.Leu244Phe