Canonical Allele Identifier: CA2811004139
Gene: AFG3L2 HGNC NCBI
TUBB6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.12337564del , CM000680.2:g.12337564del GRCh38
NC_000018.9:g.12337563del , CM000680.1:g.12337563del GRCh37
NC_000018.8:g.12327563del NCBI36
NG_023361.1:g.44713del , LRG_666:g.44713del

Transcript Alleles

HGVS Amino-acid Change
ENST00000687337.1:c.*1577-29del (AFG3L2) ENSP00000508998.1:n.*1577-29del
ENST00000687477.1:n.517-29del (AFG3L2)
ENST00000688199.1:c.1843-29del (AFG3L2) ENSP00000510237.1:n.1843-29del
ENST00000691179.1:c.1906-29del (AFG3L2) ENSP00000509010.1:n.1906-29del
ENST00000691970.1:c.*1358-29del (AFG3L2) ENSP00000508440.1:n.*1358-29del
ENST00000692497.1:c.*411-29del (AFG3L2) ENSP00000509870.1:n.*411-29del
ENST00000692988.1:n.1799-29del (AFG3L2)
ENST00000269143.8:c.1981-29del (AFG3L2) MANE Select ENSP00000269143.2:n.1981-29del
ENST00000269143.7:c.1981-29del (AFG3L2) ENSP00000269143.2:n.1981-29del
ENST00000586691.1:c.88-6485del (TUBB6)
NM_006796.2:c.1981-29del , LRG_666t1:c.1981-29del (AFG3L2) NP_006787.2:n.1981-29del
XM_011525601.1:c.1780-29del (AFG3L2) XP_011523903.1:n.1780-29del
XM_011525601.3:c.1780-29del (AFG3L2) XP_011523903.1:n.1780-29del
XR_002958227.1:n.451+662del
NM_006796.3:c.1981-29del (AFG3L2) MANE Select NP_006787.2:n.1981-29del