Canonical Allele Identifier: CA503244840

Gene: AFG3L2 TUBB6

Linked Data

• gnomAD v4: 18-12337452-A-G
• COSMIC: COSM2883694
• MyVariant Identifiers: chr18:g.12337451A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337452A>G , CM000680.2:g.12337452A>G	GRCh38
NC_000018.9:g.12337451A>G , CM000680.1:g.12337451A>G	GRCh37
NC_000018.8:g.12327451A>G	NCBI36
NG_023361.1:g.44825T>C , LRG_666:g.44825T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687337.1:c.*1660T>C (AFG3L2)	ENSP00000508998.1:n.*1660T>C
ENST00000687477.1:n.600T>C (AFG3L2)
ENST00000688199.1:c.1926T>C (AFG3L2)	ENSP00000510237.1:p.Pro642=
ENST00000691179.1:c.1989T>C (AFG3L2)	ENSP00000509010.1:p.Pro663=
ENST00000691970.1:c.*1441T>C (AFG3L2)	ENSP00000508440.1:n.*1441T>C
ENST00000692497.1:c.*494T>C (AFG3L2)	ENSP00000509870.1:n.*494T>C
ENST00000692988.1:n.1882T>C (AFG3L2)
ENST00000269143.8:c.2064T>C (AFG3L2) MANE Select	ENSP00000269143.2:p.Pro688=
ENST00000269143.7:c.2064T>C (AFG3L2)	ENSP00000269143.2:p.Pro688=
ENST00000586691.1:c.88-6597A>G (TUBB6)
NM_006796.2:c.2064T>C , LRG_666t1:c.2064T>C (AFG3L2)	NP_006787.2:p.Pro688=
XM_011525601.1:c.1863T>C (AFG3L2)	XP_011523903.1:p.Pro621=
XM_011525601.3:c.1863T>C (AFG3L2)	XP_011523903.1:p.Pro621=
XR_002958227.1:n.451+550A>G
NM_006796.3:c.2064T>C (AFG3L2) MANE Select	NP_006787.2:p.Pro688=