Canonical Allele Identifier: CA503244848
Gene: AFG3L2 HGNC NCBI
TUBB6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.12337457C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.12337458C>T , CM000680.2:g.12337458C>T GRCh38
NC_000018.9:g.12337457C>T , CM000680.1:g.12337457C>T GRCh37
NC_000018.8:g.12327457C>T NCBI36
NG_023361.1:g.44819G>A , LRG_666:g.44819G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000687337.1:c.*1654G>A (AFG3L2) ENSP00000508998.1:n.*1654G>A
ENST00000687477.1:n.594G>A (AFG3L2)
ENST00000688199.1:c.1920G>A (AFG3L2) ENSP00000510237.1:p.Glu640=
ENST00000691179.1:c.1983G>A (AFG3L2) ENSP00000509010.1:p.Glu661=
ENST00000691970.1:c.*1435G>A (AFG3L2) ENSP00000508440.1:n.*1435G>A
ENST00000692497.1:c.*488G>A (AFG3L2) ENSP00000509870.1:n.*488G>A
ENST00000692988.1:n.1876G>A (AFG3L2)
ENST00000269143.8:c.2058G>A (AFG3L2) MANE Select ENSP00000269143.2:p.Glu686=
ENST00000269143.7:c.2058G>A (AFG3L2) ENSP00000269143.2:p.Glu686=
ENST00000586691.1:c.88-6591C>T (TUBB6)
NM_006796.2:c.2058G>A , LRG_666t1:c.2058G>A (AFG3L2) NP_006787.2:p.Glu686=
XM_011525601.1:c.1857G>A (AFG3L2) XP_011523903.1:p.Glu619=
XM_011525601.3:c.1857G>A (AFG3L2) XP_011523903.1:p.Glu619=
XR_002958227.1:n.451+556C>T
NM_006796.3:c.2058G>A (AFG3L2) MANE Select NP_006787.2:p.Glu686=