Canonical Allele Identifier: CA8896276

Gene: AFG3L2 TUBB6

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337211A>T , CM000680.2:g.12337211A>T	GRCh38
NC_000018.9:g.12337210A>T , CM000680.1:g.12337210A>T	GRCh37
NC_000018.8:g.12327210A>T	NCBI36
NG_023361.1:g.45066T>A , LRG_666:g.45066T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006796.3:c.2175+130T>A (AFG3L2) MANE Select	NP_006787.2:n.2175+130T>A
ENST00000269143.8:c.2175+130T>A (AFG3L2) MANE Select	ENSP00000269143.2:n.2175+130T>A
NM_006796.2:c.2175+130T>A , LRG_666t1:c.2175+130T>A (AFG3L2)	NP_006787.2:n.2175+130T>A
ENST00000269143.7:c.2175+130T>A (AFG3L2)	ENSP00000269143.2:n.2175+130T>A
ENST00000586691.1:c.88-6838A>T (TUBB6)
ENST00000590967.5:c.*28A>T (TUBB6)	ENSP00000465386.1:n.*28A>T
ENST00000687337.1:c.*1771+130T>A (AFG3L2)	ENSP00000508998.1:n.*1771+130T>A
ENST00000687477.1:n.711+130T>A (AFG3L2)
ENST00000688199.1:c.2037+130T>A (AFG3L2)	ENSP00000510237.1:n.2037+130T>A
ENST00000691179.1:c.2100+130T>A (AFG3L2)	ENSP00000509010.1:n.2100+130T>A
ENST00000691970.1:c.*1552+130T>A (AFG3L2)	ENSP00000508440.1:n.*1552+130T>A
ENST00000692497.1:c.*605+130T>A (AFG3L2)	ENSP00000509870.1:n.*605+130T>A
ENST00000692988.1:n.1993+130T>A (AFG3L2)
XM_011525601.1:c.1974+130T>A (AFG3L2)	XP_011523903.1:n.1974+130T>A
XM_011525601.3:c.1974+130T>A (AFG3L2)	XP_011523903.1:n.1974+130T>A
XR_002958227.1:n.451+309A>T