Canonical Allele Identifier: CA2194541799

Gene: POLG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318613A= , CM000677.2:g.89318613A=	GRCh38
NC_000015.9:g.89861844A= , CM000677.1:g.89861844A=	GRCh37
NC_000015.8:g.87662848A=	NCBI36
NG_008218.1:g.21183T=
NG_011736.1:g.79651A= , LRG_500:g.79651A=
NG_008218.2:g.21183T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.3410T=	ENSP00000516154.1:p.Val1137=
ENST00000268124.11:c.3410T= MANE Select	ENSP00000268124.5:p.Val1137=
ENST00000530292.3:c.3011T=	ENSP00000432885.2:p.Val1004=
ENST00000635986.2:c.*480T=	ENSP00000490653.2:n.*480T=
ENST00000636774.1:c.*1977T=	ENSP00000489799.1:n.*1977T=
ENST00000637238.1:c.2219T=	ENSP00000490756.1:n.2219T=
ENST00000637264.1:c.2482T=
ENST00000666746.1:c.2987T=
ENST00000672071.1:n.3608T=
ENST00000672695.1:n.587T=
ENST00000672923.2:n.3410T=
ENST00000268124.9:c.3410T=	ENSP00000268124.5:p.Val1137=
ENST00000442287.6:c.3410T=	ENSP00000399851.2:p.Val1137=
ENST00000530292.2:c.494T=	ENSP00000432885.1:p.Val165=
ENST00000631044.2:c.*2834T=	ENSP00000486730.1:n.*2834T=
NM_001126131.1:c.3410T=	NP_001119603.1:p.Val1137=
NM_002693.2:c.3410T=	NP_002684.1:p.Val1137=
NM_001126131.2:c.3410T=	NP_001119603.1:p.Val1137=
NM_002693.3:c.3410T= MANE Select	NP_002684.1:p.Val1137=