Canonical Allele Identifier: CA2285198781
Gene: AFG3L2 HGNC NCBI
TUBB6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.12337397C= , CM000680.2:g.12337397C= GRCh38
NC_000018.9:g.12337396C= , CM000680.1:g.12337396C= GRCh37
NC_000018.8:g.12327396C= NCBI36
NG_023361.1:g.44880G= , LRG_666:g.44880G=

Transcript Alleles

HGVS Amino-acid change
ENST00000687337.1:c.*1715G= (AFG3L2) ENSP00000508998.1:n.*1715G=
ENST00000687477.1:n.655G= (AFG3L2)
ENST00000688199.1:c.1981G= (AFG3L2) ENSP00000510237.1:p.Asp661=
ENST00000691179.1:c.2044G= (AFG3L2) ENSP00000509010.1:p.Asp682=
ENST00000691970.1:c.*1496G= (AFG3L2) ENSP00000508440.1:n.*1496G=
ENST00000692497.1:c.*549G= (AFG3L2) ENSP00000509870.1:n.*549G=
ENST00000692988.1:n.1937G= (AFG3L2)
ENST00000269143.8:c.2119G= (AFG3L2) MANE Select ENSP00000269143.2:p.Asp707=
ENST00000269143.7:c.2119G= (AFG3L2) ENSP00000269143.2:p.Asp707=
ENST00000586691.1:c.88-6652C= (TUBB6)
NM_006796.2:c.2119G= , LRG_666t1:c.2119G= (AFG3L2) NP_006787.2:p.Asp707=
XM_011525601.1:c.1918G= (AFG3L2) XP_011523903.1:p.Asp640=
XM_011525601.3:c.1918G= (AFG3L2) XP_011523903.1:p.Asp640=
XR_002958227.1:n.451+495C=
NM_006796.3:c.2119G= (AFG3L2) MANE Select NP_006787.2:p.Asp707=