Canonical Allele Identifier: CA8712924
Community Standard Title: NM_007215.4(POLG2):c.775C>T (p.Arg259Ter)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.64492687G>A , CM000679.2:g.64492687G>A GRCh38
NC_000017.10:g.62488804G>A , CM000679.1:g.62488804G>A GRCh37
NC_000017.9:g.59919266G>A NCBI36
NG_013029.1:g.9381C>T

Transcript Alleles

HGVS Amino-acid Change
NM_007215.4:c.775C>T (POLG2) MANE Select NP_009146.2:p.Arg259Ter
ENST00000539111.7:c.775C>T (POLG2) MANE Select ENSP00000442563.2:p.Arg259Ter
NM_007215.3:c.775C>T (POLG2) NP_009146.2:p.Arg259Ter
ENST00000539111.6:c.775C>T (POLG2) ENSP00000442563.2:p.Arg259Ter
ENST00000578687.5:n.102C>T (POLG2)
ENST00000578997.1:c.437C>T (POLG2) ENSP00000464389.1:n.437C>T
ENST00000580893.5:n.213C>T (POLG2)
ENST00000581355.1:c.34C>T (POLG2) ENSP00000462071.1:p.Arg12Ter
ENST00000585104.2:n.746C>T (POLG2)
ENST00000585141.5:n.826C>T (POLG2)
ENST00000671755.1:c.746C>T (POLG2)
ENST00000673460.1:c.746C>T (POLG2)
XM_006721651.2:c.775C>T (POLG2) XP_006721714.1:p.Arg259Ter
XM_024450706.1:c.*431G>A (MILR1) XP_024306474.1:n.*431G>A
XM_024450708.1:c.*29-3634G>A (MILR1) XP_024306476.1:n.*29-3634G>A
XR_002957989.1:n.1270+340G>A (MILR1)
XR_002957990.1:n.1270+340G>A (MILR1)
XR_243630.1:n.826C>T (POLG2)
XR_934357.1:n.826C>T (POLG2)
XR_934358.1:n.826C>T (POLG2)