Canonical Allele Identifier: CA2630256592

Gene: POLG POLGARF

Linked Data

• gnomAD v4: 15-89330373-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89330373C>T , CM000677.2:g.89330373C>T	GRCh38
NC_000015.9:g.89873604C>T , CM000677.1:g.89873604C>T	GRCh37
NC_000015.8:g.87674608C>T	NCBI36
NG_008218.1:g.9423G>A
NG_008218.2:g.9423G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.660-97G>A (POLG)	ENSP00000516154.1:n.660-97G>A
ENST00000706918.1:c.715-97G>A (POLGARF)	ENSP00000516626.1:n.715-97G>A
ENST00000268124.11:c.660-97G>A (POLG) MANE Select	ENSP00000268124.5:n.660-97G>A
ENST00000530292.3:c.261-97G>A (POLG)	ENSP00000432885.2:n.261-97G>A
ENST00000635986.2:c.660-97G>A (POLG)	ENSP00000490653.2:n.660-97G>A
ENST00000636774.1:c.660-97G>A (POLG)	ENSP00000489799.1:n.660-97G>A
ENST00000637307.1:c.50-112G>A (POLG)
ENST00000650303.2:c.715-97G>A (POLG)	ENSP00000497242.2:n.715-97G>A
ENST00000666746.1:c.317-97G>A (POLG)
ENST00000672071.1:n.858-97G>A (POLG)
ENST00000268124.9:c.660-97G>A (POLG)	ENSP00000268124.5:n.660-97G>A
ENST00000442287.6:c.660-97G>A (POLG)	ENSP00000399851.2:n.660-97G>A
ENST00000631044.2:c.*43-97G>A (POLG)	ENSP00000486730.1:n.*43-97G>A
NM_001126131.1:c.660-97G>A (POLG)	NP_001119603.1:n.660-97G>A
NM_002693.2:c.660-97G>A (POLG)	NP_002684.1:n.660-97G>A
NM_001126131.2:c.660-97G>A (POLG)	NP_001119603.1:n.660-97G>A
NM_002693.3:c.660-97G>A (POLG) MANE Select	NP_002684.1:n.660-97G>A