Canonical Allele Identifier: CA401943980

Gene: AFG3L2 TUBB6

Linked Data

• MyVariant Identifiers: chr18:g.12337435C>G (hg19) ; chr18:g.12337436C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337436C>G , CM000680.2:g.12337436C>G	GRCh38
NC_000018.9:g.12337435C>G , CM000680.1:g.12337435C>G	GRCh37
NC_000018.8:g.12327435C>G	NCBI36
NG_023361.1:g.44841G>C , LRG_666:g.44841G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687337.1:c.*1676G>C (AFG3L2)	ENSP00000508998.1:n.*1676G>C
ENST00000687477.1:n.616G>C (AFG3L2)
ENST00000688199.1:c.1942G>C (AFG3L2)	ENSP00000510237.1:p.Ala648Pro
ENST00000691179.1:c.2005G>C (AFG3L2)	ENSP00000509010.1:p.Ala669Pro
ENST00000691970.1:c.*1457G>C (AFG3L2)	ENSP00000508440.1:n.*1457G>C
ENST00000692497.1:c.*510G>C (AFG3L2)	ENSP00000509870.1:n.*510G>C
ENST00000692988.1:n.1898G>C (AFG3L2)
ENST00000269143.8:c.2080G>C (AFG3L2) MANE Select	ENSP00000269143.2:p.Ala694Pro
ENST00000269143.7:c.2080G>C (AFG3L2)	ENSP00000269143.2:p.Ala694Pro
ENST00000586691.1:c.88-6613C>G (TUBB6)
NM_006796.2:c.2080G>C , LRG_666t1:c.2080G>C (AFG3L2)	NP_006787.2:p.Ala694Pro
XM_011525601.1:c.1879G>C (AFG3L2)	XP_011523903.1:p.Ala627Pro
XM_011525601.3:c.1879G>C (AFG3L2)	XP_011523903.1:p.Ala627Pro
XR_002958227.1:n.451+534C>G
NM_006796.3:c.2080G>C (AFG3L2) MANE Select	NP_006787.2:p.Ala694Pro