Canonical Allele Identifier: CA393751103

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89862302C>A (hg19) ; chr15:g.89319071C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89319071C>A , CM000677.2:g.89319071C>A	GRCh38
NC_000015.9:g.89862302C>A , CM000677.1:g.89862302C>A	GRCh37
NC_000015.8:g.87663306C>A	NCBI36
NG_008218.1:g.20725G>T
NG_011736.1:g.80109C>A , LRG_500:g.80109C>A
NG_008218.2:g.20725G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.3133G>T	ENSP00000516154.1:p.Ala1045Ser
ENST00000268124.11:c.3133G>T MANE Select	ENSP00000268124.5:p.Ala1045Ser
ENST00000530292.3:c.2734G>T	ENSP00000432885.2:p.Ala912Ser
ENST00000635986.2:c.*203G>T	ENSP00000490653.2:n.*203G>T
ENST00000636530.1:n.93G>T
ENST00000636774.1:c.*1700G>T	ENSP00000489799.1:n.*1700G>T
ENST00000637238.1:c.1942G>T	ENSP00000490756.1:n.1942G>T
ENST00000637264.1:c.2205G>T
ENST00000666746.1:c.2710G>T
ENST00000672071.1:n.3331G>T
ENST00000672695.1:n.310G>T
ENST00000672923.2:n.3133G>T
ENST00000268124.9:c.3133G>T	ENSP00000268124.5:p.Ala1045Ser
ENST00000442287.6:c.3133G>T	ENSP00000399851.2:p.Ala1045Ser
ENST00000530292.2:c.217G>T	ENSP00000432885.1:p.Ala73Ser
ENST00000631044.2:c.*2557G>T	ENSP00000486730.1:n.*2557G>T
NM_001126131.1:c.3133G>T	NP_001119603.1:p.Ala1045Ser
NM_002693.2:c.3133G>T	NP_002684.1:p.Ala1045Ser
NM_001126131.2:c.3133G>T	NP_001119603.1:p.Ala1045Ser
NM_002693.3:c.3133G>T MANE Select	NP_002684.1:p.Ala1045Ser