Canonical Allele Identifier: CA401944080

Gene: AFG3L2 TUBB6

Linked Data

• MyVariant Identifiers: chr18:g.12337456T>C (hg19) ; chr18:g.12337457T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337457T>C , CM000680.2:g.12337457T>C	GRCh38
NC_000018.9:g.12337456T>C , CM000680.1:g.12337456T>C	GRCh37
NC_000018.8:g.12327456T>C	NCBI36
NG_023361.1:g.44820A>G , LRG_666:g.44820A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687337.1:c.*1655A>G (AFG3L2)	ENSP00000508998.1:n.*1655A>G
ENST00000687477.1:n.595A>G (AFG3L2)
ENST00000688199.1:c.1921A>G (AFG3L2)	ENSP00000510237.1:p.Lys641Glu
ENST00000691179.1:c.1984A>G (AFG3L2)	ENSP00000509010.1:p.Lys662Glu
ENST00000691970.1:c.*1436A>G (AFG3L2)	ENSP00000508440.1:n.*1436A>G
ENST00000692497.1:c.*489A>G (AFG3L2)	ENSP00000509870.1:n.*489A>G
ENST00000692988.1:n.1877A>G (AFG3L2)
ENST00000269143.8:c.2059A>G (AFG3L2) MANE Select	ENSP00000269143.2:p.Lys687Glu
ENST00000269143.7:c.2059A>G (AFG3L2)	ENSP00000269143.2:p.Lys687Glu
ENST00000586691.1:c.88-6592T>C (TUBB6)
NM_006796.2:c.2059A>G , LRG_666t1:c.2059A>G (AFG3L2)	NP_006787.2:p.Lys687Glu
XM_011525601.1:c.1858A>G (AFG3L2)	XP_011523903.1:p.Lys620Glu
XM_011525601.3:c.1858A>G (AFG3L2)	XP_011523903.1:p.Lys620Glu
XR_002958227.1:n.451+555T>C
NM_006796.3:c.2059A>G (AFG3L2) MANE Select	NP_006787.2:p.Lys687Glu