Canonical Allele Identifier: CA393749964

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89861924G>T (hg19) ; chr15:g.89318693G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318693G>T , CM000677.2:g.89318693G>T	GRCh38
NC_000015.9:g.89861924G>T , CM000677.1:g.89861924G>T	GRCh37
NC_000015.8:g.87662928G>T	NCBI36
NG_008218.1:g.21103C>A
NG_011736.1:g.79731G>T , LRG_500:g.79731G>T
NG_008218.2:g.21103C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3330C>A	ENSP00000516154.1:p.His1110Gln
ENST00000268124.11:c.3330C>A MANE Select	ENSP00000268124.5:p.His1110Gln
ENST00000530292.3:c.2931C>A	ENSP00000432885.2:p.His977Gln
ENST00000635986.2:c.*400C>A	ENSP00000490653.2:n.*400C>A
ENST00000636774.1:c.*1897C>A	ENSP00000489799.1:n.*1897C>A
ENST00000637238.1:c.2139C>A	ENSP00000490756.1:n.2139C>A
ENST00000637264.1:c.2402C>A
ENST00000666746.1:c.2907C>A
ENST00000672071.1:n.3528C>A
ENST00000672695.1:n.507C>A
ENST00000672923.2:n.3330C>A
ENST00000268124.9:c.3330C>A	ENSP00000268124.5:p.His1110Gln
ENST00000442287.6:c.3330C>A	ENSP00000399851.2:p.His1110Gln
ENST00000530292.2:c.414C>A	ENSP00000432885.1:p.His138Gln
ENST00000631044.2:c.*2754C>A	ENSP00000486730.1:n.*2754C>A
NM_001126131.1:c.3330C>A	NP_001119603.1:p.His1110Gln
NM_002693.2:c.3330C>A	NP_002684.1:p.His1110Gln
NM_001126131.2:c.3330C>A	NP_001119603.1:p.His1110Gln
NM_002693.3:c.3330C>A MANE Select	NP_002684.1:p.His1110Gln