Canonical Allele Identifier: CA393747473

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89860678T>G (hg19) ; chr15:g.89317447T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89317447T>G , CM000677.2:g.89317447T>G	GRCh38
NC_000015.9:g.89860678T>G , CM000677.1:g.89860678T>G	GRCh37
NC_000015.8:g.87661682T>G	NCBI36
NG_008218.1:g.22349A>C
NG_011736.1:g.78485T>G , LRG_500:g.78485T>G
NG_008218.2:g.22349A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.3572A>C	ENSP00000516154.1:p.Lys1191Thr
ENST00000268124.11:c.3572A>C MANE Select	ENSP00000268124.5:p.Lys1191Thr
ENST00000530292.3:c.3272A>C	ENSP00000432885.2:n.3272A>C
ENST00000635986.2:c.*642A>C	ENSP00000490653.2:n.*642A>C
ENST00000636774.1:c.*2176A>C	ENSP00000489799.1:n.*2176A>C
ENST00000637042.1:n.96A>C
ENST00000637238.1:c.2480A>C	ENSP00000490756.1:n.2480A>C
ENST00000637264.1:c.2584A>C
ENST00000666746.1:c.3149A>C
ENST00000672071.1:n.4774A>C
ENST00000672695.1:n.1351A>C
ENST00000672923.2:n.3572A>C
ENST00000268124.9:c.3572A>C	ENSP00000268124.5:p.Lys1191Thr
ENST00000442287.6:c.3572A>C	ENSP00000399851.2:p.Lys1191Thr
ENST00000526671.1:n.382A>C
ENST00000530292.2:c.755A>C	ENSP00000432885.1:n.755A>C
ENST00000631044.2:c.*2996A>C	ENSP00000486730.1:n.*2996A>C
NM_001126131.1:c.3572A>C	NP_001119603.1:p.Lys1191Thr
NM_002693.2:c.3572A>C	NP_002684.1:p.Lys1191Thr
NM_001126131.2:c.3572A>C	NP_001119603.1:p.Lys1191Thr
NM_002693.3:c.3572A>C MANE Select	NP_002684.1:p.Lys1191Thr