Canonical Allele Identifier: CA393750632

Gene: POLG

Linked Data

• dbSNP Id: rs1237483748
• MyVariant Identifiers: chr15:g.89862221T>G (hg19) ; chr15:g.89318990T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318990T>G , CM000677.2:g.89318990T>G	GRCh38
NC_000015.9:g.89862221T>G , CM000677.1:g.89862221T>G	GRCh37
NC_000015.8:g.87663225T>G	NCBI36
NG_008218.1:g.20806A>C
NG_011736.1:g.80028T>G , LRG_500:g.80028T>G
NG_008218.2:g.20806A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.3214A>C	ENSP00000516154.1:p.Thr1072Pro
ENST00000268124.11:c.3214A>C MANE Select	ENSP00000268124.5:p.Thr1072Pro
ENST00000530292.3:c.2815A>C	ENSP00000432885.2:p.Thr939Pro
ENST00000635986.2:c.*284A>C	ENSP00000490653.2:n.*284A>C
ENST00000636774.1:c.*1781A>C	ENSP00000489799.1:n.*1781A>C
ENST00000637238.1:c.2023A>C	ENSP00000490756.1:n.2023A>C
ENST00000637264.1:c.2286A>C
ENST00000666746.1:c.2791A>C
ENST00000672071.1:n.3412A>C
ENST00000672695.1:n.391A>C
ENST00000672923.2:n.3214A>C
ENST00000268124.9:c.3214A>C	ENSP00000268124.5:p.Thr1072Pro
ENST00000442287.6:c.3214A>C	ENSP00000399851.2:p.Thr1072Pro
ENST00000530292.2:c.298A>C	ENSP00000432885.1:p.Thr100Pro
ENST00000631044.2:c.*2638A>C	ENSP00000486730.1:n.*2638A>C
NM_001126131.1:c.3214A>C	NP_001119603.1:p.Thr1072Pro
NM_002693.2:c.3214A>C	NP_002684.1:p.Thr1072Pro
NM_001126131.2:c.3214A>C	NP_001119603.1:p.Thr1072Pro
NM_002693.3:c.3214A>C MANE Select	NP_002684.1:p.Thr1072Pro