Canonical Allele Identifier: CA401944052

Gene: AFG3L2 TUBB6

Linked Data

• ClinVar Variation Id: 1700708
• ClinVar RCV Id: RCV002275381
• dbSNP Id: rs1598820860
• MyVariant Identifiers: chr18:g.12337450A>T (hg19) ; chr18:g.12337451A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337451A>T , CM000680.2:g.12337451A>T	GRCh38
NC_000018.9:g.12337450A>T , CM000680.1:g.12337450A>T	GRCh37
NC_000018.8:g.12327450A>T	NCBI36
NG_023361.1:g.44826T>A , LRG_666:g.44826T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687337.1:c.*1661T>A (AFG3L2)	ENSP00000508998.1:n.*1661T>A
ENST00000687477.1:n.601T>A (AFG3L2)
ENST00000688199.1:c.1927T>A (AFG3L2)	ENSP00000510237.1:p.Tyr643Asn
ENST00000691179.1:c.1990T>A (AFG3L2)	ENSP00000509010.1:p.Tyr664Asn
ENST00000691970.1:c.*1442T>A (AFG3L2)	ENSP00000508440.1:n.*1442T>A
ENST00000692497.1:c.*495T>A (AFG3L2)	ENSP00000509870.1:n.*495T>A
ENST00000692988.1:n.1883T>A (AFG3L2)
ENST00000269143.8:c.2065T>A (AFG3L2) MANE Select	ENSP00000269143.2:p.Tyr689Asn
ENST00000269143.7:c.2065T>A (AFG3L2)	ENSP00000269143.2:p.Tyr689Asn
ENST00000586691.1:c.88-6598A>T (TUBB6)
NM_006796.2:c.2065T>A , LRG_666t1:c.2065T>A (AFG3L2)	NP_006787.2:p.Tyr689Asn
XM_011525601.1:c.1864T>A (AFG3L2)	XP_011523903.1:p.Tyr622Asn
XM_011525601.3:c.1864T>A (AFG3L2)	XP_011523903.1:p.Tyr622Asn
XR_002958227.1:n.451+549A>T
NM_006796.3:c.2065T>A (AFG3L2) MANE Select	NP_006787.2:p.Tyr689Asn