Canonical Allele Identifier: CA401943772

Gene: AFG3L2 TUBB6

Linked Data

• COSMIC: COSM986606
• MyVariant Identifiers: chr18:g.12337392G>A (hg19) ; chr18:g.12337393G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337393G>A , CM000680.2:g.12337393G>A	GRCh38
NC_000018.9:g.12337392G>A , CM000680.1:g.12337392G>A	GRCh37
NC_000018.8:g.12327392G>A	NCBI36
NG_023361.1:g.44884C>T , LRG_666:g.44884C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687337.1:c.*1719C>T (AFG3L2)	ENSP00000508998.1:n.*1719C>T
ENST00000687477.1:n.659C>T (AFG3L2)
ENST00000688199.1:c.1985C>T (AFG3L2)	ENSP00000510237.1:p.Ala662Val
ENST00000691179.1:c.2048C>T (AFG3L2)	ENSP00000509010.1:p.Ala683Val
ENST00000691970.1:c.*1500C>T (AFG3L2)	ENSP00000508440.1:n.*1500C>T
ENST00000692497.1:c.*553C>T (AFG3L2)	ENSP00000509870.1:n.*553C>T
ENST00000692988.1:n.1941C>T (AFG3L2)
ENST00000269143.8:c.2123C>T (AFG3L2) MANE Select	ENSP00000269143.2:p.Ala708Val
ENST00000269143.7:c.2123C>T (AFG3L2)	ENSP00000269143.2:p.Ala708Val
ENST00000586691.1:c.88-6656G>A (TUBB6)
NM_006796.2:c.2123C>T , LRG_666t1:c.2123C>T (AFG3L2)	NP_006787.2:p.Ala708Val
XM_011525601.1:c.1922C>T (AFG3L2)	XP_011523903.1:p.Ala641Val
XM_011525601.3:c.1922C>T (AFG3L2)	XP_011523903.1:p.Ala641Val
XR_002958227.1:n.451+491G>A
NM_006796.3:c.2123C>T (AFG3L2) MANE Select	NP_006787.2:p.Ala708Val