Canonical Allele Identifier: CA401944100

Gene: AFG3L2 TUBB6

Linked Data

• gnomAD v4: 18-12337461-C-A
• MyVariant Identifiers: chr18:g.12337460C>A (hg19) ; chr18:g.12337461C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337461C>A , CM000680.2:g.12337461C>A	GRCh38
NC_000018.9:g.12337460C>A , CM000680.1:g.12337460C>A	GRCh37
NC_000018.8:g.12327460C>A	NCBI36
NG_023361.1:g.44816G>T , LRG_666:g.44816G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000687337.1:c.*1651G>T (AFG3L2)	ENSP00000508998.1:n.*1651G>T
ENST00000687477.1:n.591G>T (AFG3L2)
ENST00000688199.1:c.1917G>T (AFG3L2)	ENSP00000510237.1:p.Leu639Phe
ENST00000691179.1:c.1980G>T (AFG3L2)	ENSP00000509010.1:p.Leu660Phe
ENST00000691970.1:c.*1432G>T (AFG3L2)	ENSP00000508440.1:n.*1432G>T
ENST00000692497.1:c.*485G>T (AFG3L2)	ENSP00000509870.1:n.*485G>T
ENST00000692988.1:n.1873G>T (AFG3L2)
ENST00000269143.8:c.2055G>T (AFG3L2) MANE Select	ENSP00000269143.2:p.Leu685Phe
ENST00000269143.7:c.2055G>T (AFG3L2)	ENSP00000269143.2:p.Leu685Phe
ENST00000586691.1:c.88-6588C>A (TUBB6)
NM_006796.2:c.2055G>T , LRG_666t1:c.2055G>T (AFG3L2)	NP_006787.2:p.Leu685Phe
XM_011525601.1:c.1854G>T (AFG3L2)	XP_011523903.1:p.Leu618Phe
XM_011525601.3:c.1854G>T (AFG3L2)	XP_011523903.1:p.Leu618Phe
XR_002958227.1:n.451+559C>A
NM_006796.3:c.2055G>T (AFG3L2) MANE Select	NP_006787.2:p.Leu685Phe