Canonical Allele Identifier: CA2805169544

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323617_89323624del , CM000677.2:g.89323617_89323624del	GRCh38
NC_000015.9:g.89866848_89866855del , CM000677.1:g.89866848_89866855del	GRCh37
NC_000015.8:g.87667852_87667859del	NCBI36
NG_008218.1:g.16172_16179del
NG_008218.2:g.16172_16179del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2158-113_2158-106del	ENSP00000516154.1:n.2158-113_2158-106del
ENST00000268124.11:c.2158-113_2158-106del MANE Select	ENSP00000268124.5:n.2158-113_2158-106del
ENST00000530292.3:c.1759-113_1759-106del	ENSP00000432885.2:n.1759-113_1759-106del
ENST00000635986.2:c.2158-113_2158-106del	ENSP00000490653.2:n.2158-113_2158-106del
ENST00000636774.1:c.*725-113_*725-106del	ENSP00000489799.1:n.*725-113_*725-106del
ENST00000637238.1:c.855-113_855-106del	ENSP00000490756.1:n.855-113_855-106del
ENST00000637264.1:c.1230-113_1230-106del
ENST00000666746.1:c.1735-113_1735-106del
ENST00000670281.1:c.478-113_478-106del	ENSP00000499709.1:n.478-113_478-106del
ENST00000672071.1:n.2356-113_2356-106del
ENST00000672923.2:n.2261-113_2261-106del
ENST00000268124.9:c.2158-113_2158-106del	ENSP00000268124.5:n.2158-113_2158-106del
ENST00000442287.6:c.2158-113_2158-106del	ENSP00000399851.2:n.2158-113_2158-106del
ENST00000526314.2:c.539+191_539+198del
ENST00000526398.1:c.307-113_307-106del
ENST00000526573.1:n.434_441del
ENST00000532584.5:n.360-113_360-106del
ENST00000533857.1:n.463_470del
ENST00000631044.2:c.*1541-72_*1541-65del	ENSP00000486730.1:n.*1541-72_*1541-65del
NM_001126131.1:c.2158-113_2158-106del	NP_001119603.1:n.2158-113_2158-106del
NM_002693.2:c.2158-113_2158-106del	NP_002684.1:n.2158-113_2158-106del
NM_001126131.2:c.2158-113_2158-106del	NP_001119603.1:n.2158-113_2158-106del
NM_002693.3:c.2158-113_2158-106del MANE Select	NP_002684.1:n.2158-113_2158-106del