Canonical Allele Identifier: CA2285198954
Gene: AFG3L2 HGNC NCBI
TUBB6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.12337506A= , CM000680.2:g.12337506A= GRCh38
NC_000018.9:g.12337505A= , CM000680.1:g.12337505A= GRCh37
NC_000018.8:g.12327505A= NCBI36
NG_023361.1:g.44771T= , LRG_666:g.44771T=

Transcript Alleles

HGVS Amino-acid change
ENST00000687337.1:c.*1606T= (AFG3L2) ENSP00000508998.1:n.*1606T=
ENST00000687477.1:n.546T= (AFG3L2)
ENST00000688199.1:c.1872T= (AFG3L2) ENSP00000510237.1:p.Val624=
ENST00000691179.1:c.1935T= (AFG3L2) ENSP00000509010.1:p.Val645=
ENST00000691970.1:c.*1387T= (AFG3L2) ENSP00000508440.1:n.*1387T=
ENST00000692497.1:c.*440T= (AFG3L2) ENSP00000509870.1:n.*440T=
ENST00000692988.1:n.1828T= (AFG3L2)
ENST00000269143.8:c.2010T= (AFG3L2) MANE Select ENSP00000269143.2:p.Val670=
ENST00000269143.7:c.2010T= (AFG3L2) ENSP00000269143.2:p.Val670=
ENST00000586691.1:c.88-6543A= (TUBB6)
NM_006796.2:c.2010T= , LRG_666t1:c.2010T= (AFG3L2) NP_006787.2:p.Val670=
XM_011525601.1:c.1809T= (AFG3L2) XP_011523903.1:p.Val603=
XM_011525601.3:c.1809T= (AFG3L2) XP_011523903.1:p.Val603=
XR_002958227.1:n.451+604A=
NM_006796.3:c.2010T= (AFG3L2) MANE Select NP_006787.2:p.Val670=