Canonical Allele Identifier: CA393749716

Gene: POLG

Linked Data

• MyVariant Identifiers: chr15:g.89861808G>A (hg19) ; chr15:g.89318577G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89318577G>A , CM000677.2:g.89318577G>A	GRCh38
NC_000015.9:g.89861808G>A , CM000677.1:g.89861808G>A	GRCh37
NC_000015.8:g.87662812G>A	NCBI36
NG_008218.1:g.21219C>T
NG_011736.1:g.79615G>A , LRG_500:g.79615G>A
NG_008218.2:g.21219C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.3446C>T	ENSP00000516154.1:p.Ala1149Val
ENST00000268124.11:c.3446C>T MANE Select	ENSP00000268124.5:p.Ala1149Val
ENST00000530292.3:c.3047C>T	ENSP00000432885.2:p.Ala1016Val
ENST00000635986.2:c.*516C>T	ENSP00000490653.2:n.*516C>T
ENST00000636774.1:c.*2013C>T	ENSP00000489799.1:n.*2013C>T
ENST00000637238.1:c.2255C>T	ENSP00000490756.1:n.2255C>T
ENST00000637264.1:c.2518C>T
ENST00000666746.1:c.3023C>T
ENST00000672071.1:n.3644C>T
ENST00000672695.1:n.623C>T
ENST00000672923.2:n.3446C>T
ENST00000268124.9:c.3446C>T	ENSP00000268124.5:p.Ala1149Val
ENST00000442287.6:c.3446C>T	ENSP00000399851.2:p.Ala1149Val
ENST00000530292.2:c.530C>T	ENSP00000432885.1:p.Ala177Val
ENST00000631044.2:c.*2870C>T	ENSP00000486730.1:n.*2870C>T
NM_001126131.1:c.3446C>T	NP_001119603.1:p.Ala1149Val
NM_002693.2:c.3446C>T	NP_002684.1:p.Ala1149Val
NM_001126131.2:c.3446C>T	NP_001119603.1:p.Ala1149Val
NM_002693.3:c.3446C>T MANE Select	NP_002684.1:p.Ala1149Val