Canonical Allele Identifier: CA393758991

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89868702G>A (hg19) ; chr15:g.89325471G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325471G>A , CM000677.2:g.89325471G>A	GRCh38
NC_000015.9:g.89868702G>A , CM000677.1:g.89868702G>A	GRCh37
NC_000015.8:g.87669706G>A	NCBI36
NG_008218.1:g.14325C>T
NG_008218.2:g.14325C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1928C>T	ENSP00000516154.1:p.Ala643Val
ENST00000268124.11:c.1928C>T MANE Select	ENSP00000268124.5:p.Ala643Val
ENST00000530292.3:c.1529C>T	ENSP00000432885.2:p.Ala510Val
ENST00000635986.2:c.1928C>T	ENSP00000490653.2:p.Ala643Val
ENST00000636774.1:c.*495C>T	ENSP00000489799.1:n.*495C>T
ENST00000637238.1:c.646+19C>T	ENSP00000490756.1:n.646+19C>T
ENST00000637264.1:c.1000C>T
ENST00000666746.1:c.1505C>T
ENST00000670281.1:c.248C>T	ENSP00000499709.1:p.Ala83Val
ENST00000672071.1:n.2126C>T
ENST00000672923.2:n.2031C>T
ENST00000268124.9:c.1928C>T	ENSP00000268124.5:p.Ala643Val
ENST00000442287.6:c.1928C>T	ENSP00000399851.2:p.Ala643Val
ENST00000526314.2:c.310C>T
ENST00000526398.1:c.117C>T
ENST00000526573.1:n.14C>T
ENST00000532584.5:n.130C>T
ENST00000631044.2:c.*1311C>T	ENSP00000486730.1:n.*1311C>T
NM_001126131.1:c.1928C>T	NP_001119603.1:p.Ala643Val
NM_002693.2:c.1928C>T	NP_002684.1:p.Ala643Val
NM_001126131.2:c.1928C>T	NP_001119603.1:p.Ala643Val
NM_002693.3:c.1928C>T MANE Select	NP_002684.1:p.Ala643Val