Canonical Allele Identifier: CA2805168371
Gene: POLG HGNC NCBI
POLGARF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89333240_89333241del , CM000677.2:g.89333240_89333241del GRCh38
NC_000015.9:g.89876471_89876472del , CM000677.1:g.89876471_89876472del GRCh37
NC_000015.8:g.87677475_87677476del NCBI36
NG_008218.1:g.6556_6557del
NG_008218.2:g.6556_6557del

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.515_516del (POLG) ENSP00000516154.1:p.Ala172GlyfsTer?
ENST00000706918.1:c.570_571del (POLGARF) ENSP00000516626.1:p.Gly191ArgfsTer?
ENST00000268124.11:c.515_516del (POLG) MANE Select ENSP00000268124.5:p.Ala172GlyfsTer?
ENST00000530292.3:c.116_117del (POLG) ENSP00000432885.2:p.Ala39GlyfsTer?
ENST00000635986.2:c.515_516del (POLG) ENSP00000490653.2:p.Ala172GlyfsTer?
ENST00000636774.1:c.515_516del (POLG) ENSP00000489799.1:p.Ala172GlyfsTer?
ENST00000650303.2:c.570_571del (POLG) ENSP00000497242.2:p.Gly191ArgfsTer?
ENST00000666746.1:c.172_173del (POLG)
ENST00000672071.1:n.713_714del (POLG)
ENST00000268124.9:c.515_516del (POLG) ENSP00000268124.5:p.Ala172GlyfsTer?
ENST00000442287.6:c.515_516del (POLG) ENSP00000399851.2:p.Ala172GlyfsTer?
ENST00000631044.2:c.515_516del (POLG) ENSP00000486730.1:p.Ala172GlyfsTer?
NM_001126131.1:c.515_516del (POLG) NP_001119603.1:p.Ala172GlyfsTer?
NM_002693.2:c.515_516del (POLG) NP_002684.1:p.Ala172GlyfsTer?
NM_001126131.2:c.515_516del (POLG) NP_001119603.1:p.Ala172GlyfsTer?
NM_002693.3:c.515_516del (POLG) MANE Select NP_002684.1:p.Ala172GlyfsTer?