Canonical Allele Identifier: CA2194542081

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318700T= , CM000677.2:g.89318700T=	GRCh38
NC_000015.9:g.89861931T= , CM000677.1:g.89861931T=	GRCh37
NC_000015.8:g.87662935T=	NCBI36
NG_008218.1:g.21096A=
NG_011736.1:g.79738T= , LRG_500:g.79738T=
NG_008218.2:g.21096A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3323A=	ENSP00000516154.1:p.Tyr1108=
ENST00000268124.11:c.3323A= MANE Select	ENSP00000268124.5:p.Tyr1108=
ENST00000530292.3:c.2924A=	ENSP00000432885.2:p.Tyr975=
ENST00000635986.2:c.*393A=	ENSP00000490653.2:n.*393A=
ENST00000636774.1:c.*1890A=	ENSP00000489799.1:n.*1890A=
ENST00000637238.1:c.2132A=	ENSP00000490756.1:n.2132A=
ENST00000637264.1:c.2395A=
ENST00000666746.1:c.2900A=
ENST00000672071.1:n.3521A=
ENST00000672695.1:n.500A=
ENST00000672923.2:n.3323A=
ENST00000268124.9:c.3323A=	ENSP00000268124.5:p.Tyr1108=
ENST00000442287.6:c.3323A=	ENSP00000399851.2:p.Tyr1108=
ENST00000530292.2:c.407A=	ENSP00000432885.1:p.Tyr136=
ENST00000631044.2:c.*2747A=	ENSP00000486730.1:n.*2747A=
NM_001126131.1:c.3323A=	NP_001119603.1:p.Tyr1108=
NM_002693.2:c.3323A=	NP_002684.1:p.Tyr1108=
NM_001126131.2:c.3323A=	NP_001119603.1:p.Tyr1108=
NM_002693.3:c.3323A= MANE Select	NP_002684.1:p.Tyr1108=