Canonical Allele Identifier: CA2285198789
Gene: AFG3L2 HGNC NCBI
TUBB6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.12337402A= , CM000680.2:g.12337402A= GRCh38
NC_000018.9:g.12337401A= , CM000680.1:g.12337401A= GRCh37
NC_000018.8:g.12327401A= NCBI36
NG_023361.1:g.44875T= , LRG_666:g.44875T=

Transcript Alleles

HGVS Amino-acid change
ENST00000687337.1:c.*1710T= (AFG3L2) ENSP00000508998.1:n.*1710T=
ENST00000687477.1:n.650T= (AFG3L2)
ENST00000688199.1:c.1976T= (AFG3L2) ENSP00000510237.1:p.Ile659=
ENST00000691179.1:c.2039T= (AFG3L2) ENSP00000509010.1:p.Ile680=
ENST00000691970.1:c.*1491T= (AFG3L2) ENSP00000508440.1:n.*1491T=
ENST00000692497.1:c.*544T= (AFG3L2) ENSP00000509870.1:n.*544T=
ENST00000692988.1:n.1932T= (AFG3L2)
ENST00000269143.8:c.2114T= (AFG3L2) MANE Select ENSP00000269143.2:p.Ile705=
ENST00000269143.7:c.2114T= (AFG3L2) ENSP00000269143.2:p.Ile705=
ENST00000586691.1:c.88-6647A= (TUBB6)
NM_006796.2:c.2114T= , LRG_666t1:c.2114T= (AFG3L2) NP_006787.2:p.Ile705=
XM_011525601.1:c.1913T= (AFG3L2) XP_011523903.1:p.Ile638=
XM_011525601.3:c.1913T= (AFG3L2) XP_011523903.1:p.Ile638=
XR_002958227.1:n.451+500A=
NM_006796.3:c.2114T= (AFG3L2) MANE Select NP_006787.2:p.Ile705=