Canonical Allele Identifier: CA393766955

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89873400G>A (hg19) ; chr15:g.89330169G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89330169G>A , CM000677.2:g.89330169G>A	GRCh38
NC_000015.9:g.89873400G>A , CM000677.1:g.89873400G>A	GRCh37
NC_000015.8:g.87674404G>A	NCBI36
NG_008218.1:g.9627C>T
NG_008218.2:g.9627C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.767C>T	ENSP00000516154.1:p.Pro256Leu
ENST00000268124.11:c.767C>T MANE Select	ENSP00000268124.5:p.Pro256Leu
ENST00000530292.3:c.368C>T	ENSP00000432885.2:p.Pro123Leu
ENST00000635986.2:c.767C>T	ENSP00000490653.2:p.Pro256Leu
ENST00000636774.1:c.767C>T	ENSP00000489799.1:p.Pro256Leu
ENST00000666746.1:c.424C>T
ENST00000672071.1:n.965C>T
ENST00000268124.9:c.767C>T	ENSP00000268124.5:p.Pro256Leu
ENST00000442287.6:c.767C>T	ENSP00000399851.2:p.Pro256Leu
ENST00000631044.2:c.*150C>T	ENSP00000486730.1:n.*150C>T
NM_001126131.1:c.767C>T	NP_001119603.1:p.Pro256Leu
NM_002693.2:c.767C>T	NP_002684.1:p.Pro256Leu
NM_001126131.2:c.767C>T	NP_001119603.1:p.Pro256Leu
NM_002693.3:c.767C>T MANE Select	NP_002684.1:p.Pro256Leu