Canonical Allele Identifier: CA401943840

Gene: AFG3L2 TUBB6

Linked Data

• MyVariant Identifiers: chr18:g.12337405G>T (hg19) ; chr18:g.12337406G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337406G>T , CM000680.2:g.12337406G>T	GRCh38
NC_000018.9:g.12337405G>T , CM000680.1:g.12337405G>T	GRCh37
NC_000018.8:g.12327405G>T	NCBI36
NG_023361.1:g.44871C>A , LRG_666:g.44871C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000687337.1:c.*1706C>A (AFG3L2)	ENSP00000508998.1:n.*1706C>A
ENST00000687477.1:n.646C>A (AFG3L2)
ENST00000688199.1:c.1972C>A (AFG3L2)	ENSP00000510237.1:p.Leu658Ile
ENST00000691179.1:c.2035C>A (AFG3L2)	ENSP00000509010.1:p.Leu679Ile
ENST00000691970.1:c.*1487C>A (AFG3L2)	ENSP00000508440.1:n.*1487C>A
ENST00000692497.1:c.*540C>A (AFG3L2)	ENSP00000509870.1:n.*540C>A
ENST00000692988.1:n.1928C>A (AFG3L2)
ENST00000269143.8:c.2110C>A (AFG3L2) MANE Select	ENSP00000269143.2:p.Leu704Ile
ENST00000269143.7:c.2110C>A (AFG3L2)	ENSP00000269143.2:p.Leu704Ile
ENST00000586691.1:c.88-6643G>T (TUBB6)
NM_006796.2:c.2110C>A , LRG_666t1:c.2110C>A (AFG3L2)	NP_006787.2:p.Leu704Ile
XM_011525601.1:c.1909C>A (AFG3L2)	XP_011523903.1:p.Leu637Ile
XM_011525601.3:c.1909C>A (AFG3L2)	XP_011523903.1:p.Leu637Ile
XR_002958227.1:n.451+504G>T
NM_006796.3:c.2110C>A (AFG3L2) MANE Select	NP_006787.2:p.Leu704Ile