Canonical Allele Identifier: CA401944257

Gene: AFG3L2 TUBB6

Linked Data

• MyVariant Identifiers: chr18:g.12337494G>C (hg19) ; chr18:g.12337495G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337495G>C , CM000680.2:g.12337495G>C	GRCh38
NC_000018.9:g.12337494G>C , CM000680.1:g.12337494G>C	GRCh37
NC_000018.8:g.12327494G>C	NCBI36
NG_023361.1:g.44782C>G , LRG_666:g.44782C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000687337.1:c.*1617C>G (AFG3L2)	ENSP00000508998.1:n.*1617C>G
ENST00000687477.1:n.557C>G (AFG3L2)
ENST00000688199.1:c.1883C>G (AFG3L2)	ENSP00000510237.1:p.Ser628Cys
ENST00000691179.1:c.1946C>G (AFG3L2)	ENSP00000509010.1:p.Ser649Cys
ENST00000691970.1:c.*1398C>G (AFG3L2)	ENSP00000508440.1:n.*1398C>G
ENST00000692497.1:c.*451C>G (AFG3L2)	ENSP00000509870.1:n.*451C>G
ENST00000692988.1:n.1839C>G (AFG3L2)
ENST00000269143.8:c.2021C>G (AFG3L2) MANE Select	ENSP00000269143.2:p.Ser674Cys
ENST00000269143.7:c.2021C>G (AFG3L2)	ENSP00000269143.2:p.Ser674Cys
ENST00000586691.1:c.88-6554G>C (TUBB6)
NM_006796.2:c.2021C>G , LRG_666t1:c.2021C>G (AFG3L2)	NP_006787.2:p.Ser674Cys
XM_011525601.1:c.1820C>G (AFG3L2)	XP_011523903.1:p.Ser607Cys
XM_011525601.3:c.1820C>G (AFG3L2)	XP_011523903.1:p.Ser607Cys
XR_002958227.1:n.451+593G>C
NM_006796.3:c.2021C>G (AFG3L2) MANE Select	NP_006787.2:p.Ser674Cys