Canonical Allele Identifier: CA393756700

Gene: POLG

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323439T>G , CM000677.2:g.89323439T>G	GRCh38
NC_000015.9:g.89866670T>G , CM000677.1:g.89866670T>G	GRCh37
NC_000015.8:g.87667674T>G	NCBI36
NG_008218.1:g.16357A>C
NG_008218.2:g.16357A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2230A>C	ENSP00000516154.1:p.Ile744Leu
ENST00000268124.11:c.2230A>C MANE Select	ENSP00000268124.5:p.Ile744Leu
ENST00000530292.3:c.1831A>C	ENSP00000432885.2:p.Ile611Leu
ENST00000635986.2:c.2230A>C	ENSP00000490653.2:p.Ile744Leu
ENST00000636774.1:c.*797A>C	ENSP00000489799.1:n.*797A>C
ENST00000637238.1:c.927A>C	ENSP00000490756.1:n.927A>C
ENST00000637264.1:c.1302A>C
ENST00000666746.1:c.1807A>C
ENST00000670281.1:c.550A>C	ENSP00000499709.1:p.Ile184Leu
ENST00000672071.1:n.2428A>C
ENST00000672923.2:n.2333A>C
ENST00000268124.9:c.2230A>C	ENSP00000268124.5:p.Ile744Leu
ENST00000442287.6:c.2230A>C	ENSP00000399851.2:p.Ile744Leu
ENST00000526314.2:c.539+376A>C
ENST00000526398.1:c.379A>C
ENST00000532584.5:n.432A>C
ENST00000631044.2:c.*1654A>C	ENSP00000486730.1:n.*1654A>C
NM_001126131.1:c.2230A>C	NP_001119603.1:p.Ile744Leu
NM_002693.2:c.2230A>C	NP_002684.1:p.Ile744Leu
NM_001126131.2:c.2230A>C	NP_001119603.1:p.Ile744Leu
NM_002693.3:c.2230A>C MANE Select	NP_002684.1:p.Ile744Leu