Canonical Allele Identifier: CA401944346

Gene: AFG3L2 TUBB6

Linked Data

• MyVariant Identifiers: chr18:g.12337512T>G (hg19) ; chr18:g.12337513T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337513T>G , CM000680.2:g.12337513T>G	GRCh38
NC_000018.9:g.12337512T>G , CM000680.1:g.12337512T>G	GRCh37
NC_000018.8:g.12327512T>G	NCBI36
NG_023361.1:g.44764A>C , LRG_666:g.44764A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687337.1:c.*1599A>C (AFG3L2)	ENSP00000508998.1:n.*1599A>C
ENST00000687477.1:n.539A>C (AFG3L2)
ENST00000688199.1:c.1865A>C (AFG3L2)	ENSP00000510237.1:p.Glu622Ala
ENST00000691179.1:c.1928A>C (AFG3L2)	ENSP00000509010.1:p.Glu643Ala
ENST00000691970.1:c.*1380A>C (AFG3L2)	ENSP00000508440.1:n.*1380A>C
ENST00000692497.1:c.*433A>C (AFG3L2)	ENSP00000509870.1:n.*433A>C
ENST00000692988.1:n.1821A>C (AFG3L2)
ENST00000269143.8:c.2003A>C (AFG3L2) MANE Select	ENSP00000269143.2:p.Glu668Ala
ENST00000269143.7:c.2003A>C (AFG3L2)	ENSP00000269143.2:p.Glu668Ala
ENST00000586691.1:c.88-6536T>G (TUBB6)
NM_006796.2:c.2003A>C , LRG_666t1:c.2003A>C (AFG3L2)	NP_006787.2:p.Glu668Ala
XM_011525601.1:c.1802A>C (AFG3L2)	XP_011523903.1:p.Glu601Ala
XM_011525601.3:c.1802A>C (AFG3L2)	XP_011523903.1:p.Glu601Ala
XR_002958227.1:n.451+611T>G
NM_006796.3:c.2003A>C (AFG3L2) MANE Select	NP_006787.2:p.Glu668Ala