Canonical Allele Identifier: CA2805168372
Gene: POLG HGNC NCBI
POLGARF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89333357del , CM000677.2:g.89333357del GRCh38
NC_000015.9:g.89876588del , CM000677.1:g.89876588del GRCh37
NC_000015.8:g.87677592del NCBI36
NG_008218.1:g.6439del
NG_008218.2:g.6439del

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.398del (POLG) ENSP00000516154.1:p.Asp133AlafsTer?
ENST00000706918.1:c.453del (POLGARF) ENSP00000516626.1:p.Gln152AsnfsTer?
ENST00000268124.11:c.398del (POLG) MANE Select ENSP00000268124.5:p.Asp133AlafsTer?
ENST00000635986.2:c.398del (POLG) ENSP00000490653.2:p.Asp133AlafsTer?
ENST00000636774.1:c.398del (POLG) ENSP00000489799.1:p.Asp133AlafsTer?
ENST00000650303.2:c.453del (POLG) ENSP00000497242.2:p.Gln152AsnfsTer?
ENST00000666746.1:c.55del (POLG)
ENST00000672071.1:n.596del (POLG)
ENST00000268124.9:c.398del (POLG) ENSP00000268124.5:p.Asp133AlafsTer?
ENST00000442287.6:c.398del (POLG) ENSP00000399851.2:p.Asp133AlafsTer?
ENST00000631044.2:c.398del (POLG) ENSP00000486730.1:p.Asp133AlafsTer?
NM_001126131.1:c.398del (POLG) NP_001119603.1:p.Asp133AlafsTer?
NM_002693.2:c.398del (POLG) NP_002684.1:p.Asp133AlafsTer?
NM_001126131.2:c.398del (POLG) NP_001119603.1:p.Asp133AlafsTer?
NM_002693.3:c.398del (POLG) MANE Select NP_002684.1:p.Asp133AlafsTer?