Canonical Allele Identifier: CA2285200411
Community Standard Title: NM_006796.3(AFG3L2):c.1976C= (p.Ala659=)
Gene: AFG3L2 HGNC NCBI
TUBB6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.12340205G= , CM000680.2:g.12340205G= GRCh38
NC_000018.9:g.12340204G= , CM000680.1:g.12340204G= GRCh37
NC_000018.8:g.12330204G= NCBI36
NG_023361.1:g.42072C= , LRG_666:g.42072C=

Transcript Alleles

HGVS Amino-acid Change
NM_006796.3:c.1976C= (AFG3L2) MANE Select NP_006787.2:p.Ala659=
ENST00000269143.8:c.1976C= (AFG3L2) MANE Select ENSP00000269143.2:p.Ala659=
NM_006796.2:c.1976C= , LRG_666t1:c.1976C= (AFG3L2) NP_006787.2:p.Ala659=
ENST00000269143.7:c.1976C= (AFG3L2) ENSP00000269143.2:p.Ala659=
ENST00000586691.1:c.88-3844G= (TUBB6)
ENST00000687337.1:c.*1572C= (AFG3L2) ENSP00000508998.1:n.*1572C=
ENST00000687477.1:n.512C= (AFG3L2)
ENST00000688199.1:c.1838C= (AFG3L2) ENSP00000510237.1:p.Ala613=
ENST00000691179.1:c.1901C= (AFG3L2) ENSP00000509010.1:p.Ala634=
ENST00000691970.1:c.*1353C= (AFG3L2) ENSP00000508440.1:n.*1353C=
ENST00000692497.1:c.*406C= (AFG3L2) ENSP00000509870.1:n.*406C=
ENST00000692988.1:n.1794C= (AFG3L2)
XM_011525601.1:c.1780-2670C= (AFG3L2) XP_011523903.1:n.1780-2670C=
XM_011525601.3:c.1780-2670C= (AFG3L2) XP_011523903.1:n.1780-2670C=
XR_001753363.1:n.415+1625G=
XR_002958227.1:n.451+3303G=