Canonical Allele Identifier: CA401943751

Gene: AFG3L2 TUBB6

Linked Data

• MyVariant Identifiers: chr18:g.12337387T>G (hg19) ; chr18:g.12337388T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337388T>G , CM000680.2:g.12337388T>G	GRCh38
NC_000018.9:g.12337387T>G , CM000680.1:g.12337387T>G	GRCh37
NC_000018.8:g.12327387T>G	NCBI36
NG_023361.1:g.44889A>C , LRG_666:g.44889A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687337.1:c.*1724A>C (AFG3L2)	ENSP00000508998.1:n.*1724A>C
ENST00000687477.1:n.664A>C (AFG3L2)
ENST00000688199.1:c.1990A>C (AFG3L2)	ENSP00000510237.1:p.Lys664Gln
ENST00000691179.1:c.2053A>C (AFG3L2)	ENSP00000509010.1:p.Lys685Gln
ENST00000691970.1:c.*1505A>C (AFG3L2)	ENSP00000508440.1:n.*1505A>C
ENST00000692497.1:c.*558A>C (AFG3L2)	ENSP00000509870.1:n.*558A>C
ENST00000692988.1:n.1946A>C (AFG3L2)
ENST00000269143.8:c.2128A>C (AFG3L2) MANE Select	ENSP00000269143.2:p.Lys710Gln
ENST00000269143.7:c.2128A>C (AFG3L2)	ENSP00000269143.2:p.Lys710Gln
ENST00000586691.1:c.88-6661T>G (TUBB6)
NM_006796.2:c.2128A>C , LRG_666t1:c.2128A>C (AFG3L2)	NP_006787.2:p.Lys710Gln
XM_011525601.1:c.1927A>C (AFG3L2)	XP_011523903.1:p.Lys643Gln
XM_011525601.3:c.1927A>C (AFG3L2)	XP_011523903.1:p.Lys643Gln
XR_002958227.1:n.451+486T>G
NM_006796.3:c.2128A>C (AFG3L2) MANE Select	NP_006787.2:p.Lys710Gln