Canonical Allele Identifier: CA401943783

Gene: AFG3L2 TUBB6

Linked Data

• MyVariant Identifiers: chr18:g.12337393C>T (hg19) ; chr18:g.12337394C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337394C>T , CM000680.2:g.12337394C>T	GRCh38
NC_000018.9:g.12337393C>T , CM000680.1:g.12337393C>T	GRCh37
NC_000018.8:g.12327393C>T	NCBI36
NG_023361.1:g.44883G>A , LRG_666:g.44883G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000687337.1:c.*1718G>A (AFG3L2)	ENSP00000508998.1:n.*1718G>A
ENST00000687477.1:n.658G>A (AFG3L2)
ENST00000688199.1:c.1984G>A (AFG3L2)	ENSP00000510237.1:p.Ala662Thr
ENST00000691179.1:c.2047G>A (AFG3L2)	ENSP00000509010.1:p.Ala683Thr
ENST00000691970.1:c.*1499G>A (AFG3L2)	ENSP00000508440.1:n.*1499G>A
ENST00000692497.1:c.*552G>A (AFG3L2)	ENSP00000509870.1:n.*552G>A
ENST00000692988.1:n.1940G>A (AFG3L2)
ENST00000269143.8:c.2122G>A (AFG3L2) MANE Select	ENSP00000269143.2:p.Ala708Thr
ENST00000269143.7:c.2122G>A (AFG3L2)	ENSP00000269143.2:p.Ala708Thr
ENST00000586691.1:c.88-6655C>T (TUBB6)
NM_006796.2:c.2122G>A , LRG_666t1:c.2122G>A (AFG3L2)	NP_006787.2:p.Ala708Thr
XM_011525601.1:c.1921G>A (AFG3L2)	XP_011523903.1:p.Ala641Thr
XM_011525601.3:c.1921G>A (AFG3L2)	XP_011523903.1:p.Ala641Thr
XR_002958227.1:n.451+492C>T
NM_006796.3:c.2122G>A (AFG3L2) MANE Select	NP_006787.2:p.Ala708Thr