Canonical Allele Identifier: CA393767087

Gene: POLG POLGARF

Linked Data

• COSMIC: COSM5624310
• MyVariant Identifiers: chr15:g.89873448G>T (hg19) ; chr15:g.89330217G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89330217G>T , CM000677.2:g.89330217G>T	GRCh38
NC_000015.9:g.89873448G>T , CM000677.1:g.89873448G>T	GRCh37
NC_000015.8:g.87674452G>T	NCBI36
NG_008218.1:g.9579C>A
NG_008218.2:g.9579C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.719C>A (POLG)	ENSP00000516154.1:p.Ser240Ter
ENST00000706918.1:c.774C>A (POLGARF)	ENSP00000516626.1:p.Val258=
ENST00000268124.11:c.719C>A (POLG) MANE Select	ENSP00000268124.5:p.Ser240Ter
ENST00000530292.3:c.320C>A (POLG)	ENSP00000432885.2:p.Ser107Ter
ENST00000635986.2:c.719C>A (POLG)	ENSP00000490653.2:p.Ser240Ter
ENST00000636774.1:c.719C>A (POLG)	ENSP00000489799.1:p.Ser240Ter
ENST00000637307.1:c.94C>A (POLG)
ENST00000650303.2:c.774C>A (POLG)	ENSP00000497242.2:p.Val258=
ENST00000666746.1:c.376C>A (POLG)
ENST00000672071.1:n.917C>A (POLG)
ENST00000268124.9:c.719C>A (POLG)	ENSP00000268124.5:p.Ser240Ter
ENST00000442287.6:c.719C>A (POLG)	ENSP00000399851.2:p.Ser240Ter
ENST00000631044.2:c.*102C>A (POLG)	ENSP00000486730.1:n.*102C>A
NM_001126131.1:c.719C>A (POLG)	NP_001119603.1:p.Ser240Ter
NM_002693.2:c.719C>A (POLG)	NP_002684.1:p.Ser240Ter
NM_001126131.2:c.719C>A (POLG)	NP_001119603.1:p.Ser240Ter
NM_002693.3:c.719C>A (POLG) MANE Select	NP_002684.1:p.Ser240Ter