Canonical Allele Identifier: CA401944389

Gene: AFG3L2 TUBB6

Linked Data

• MyVariant Identifiers: chr18:g.12337521C>T (hg19) ; chr18:g.12337522C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337522C>T , CM000680.2:g.12337522C>T	GRCh38
NC_000018.9:g.12337521C>T , CM000680.1:g.12337521C>T	GRCh37
NC_000018.8:g.12327521C>T	NCBI36
NG_023361.1:g.44755G>A , LRG_666:g.44755G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687337.1:c.*1590G>A (AFG3L2)	ENSP00000508998.1:n.*1590G>A
ENST00000687477.1:n.530G>A (AFG3L2)
ENST00000688199.1:c.1856G>A (AFG3L2)	ENSP00000510237.1:p.Gly619Asp
ENST00000691179.1:c.1919G>A (AFG3L2)	ENSP00000509010.1:p.Gly640Asp
ENST00000691970.1:c.*1371G>A (AFG3L2)	ENSP00000508440.1:n.*1371G>A
ENST00000692497.1:c.*424G>A (AFG3L2)	ENSP00000509870.1:n.*424G>A
ENST00000692988.1:n.1812G>A (AFG3L2)
ENST00000269143.8:c.1994G>A (AFG3L2) MANE Select	ENSP00000269143.2:p.Gly665Asp
ENST00000269143.7:c.1994G>A (AFG3L2)	ENSP00000269143.2:p.Gly665Asp
ENST00000586691.1:c.88-6527C>T (TUBB6)
NM_006796.2:c.1994G>A , LRG_666t1:c.1994G>A (AFG3L2)	NP_006787.2:p.Gly665Asp
XM_011525601.1:c.1793G>A (AFG3L2)	XP_011523903.1:p.Gly598Asp
XM_011525601.3:c.1793G>A (AFG3L2)	XP_011523903.1:p.Gly598Asp
XR_002958227.1:n.451+620C>T
NM_006796.3:c.1994G>A (AFG3L2) MANE Select	NP_006787.2:p.Gly665Asp