Canonical Allele Identifier: CA401943631

Gene: AFG3L2 TUBB6

Linked Data

• MyVariant Identifiers: chr18:g.12337360T>C (hg19) ; chr18:g.12337361T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337361T>C , CM000680.2:g.12337361T>C	GRCh38
NC_000018.9:g.12337360T>C , CM000680.1:g.12337360T>C	GRCh37
NC_000018.8:g.12327360T>C	NCBI36
NG_023361.1:g.44916A>G , LRG_666:g.44916A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687337.1:c.*1751A>G (AFG3L2)	ENSP00000508998.1:n.*1751A>G
ENST00000687477.1:n.691A>G (AFG3L2)
ENST00000688199.1:c.2017A>G (AFG3L2)	ENSP00000510237.1:p.Lys673Glu
ENST00000691179.1:c.2080A>G (AFG3L2)	ENSP00000509010.1:p.Lys694Glu
ENST00000691970.1:c.*1532A>G (AFG3L2)	ENSP00000508440.1:n.*1532A>G
ENST00000692497.1:c.*585A>G (AFG3L2)	ENSP00000509870.1:n.*585A>G
ENST00000692988.1:n.1973A>G (AFG3L2)
ENST00000269143.8:c.2155A>G (AFG3L2) MANE Select	ENSP00000269143.2:p.Lys719Glu
ENST00000269143.7:c.2155A>G (AFG3L2)	ENSP00000269143.2:p.Lys719Glu
ENST00000586691.1:c.88-6688T>C (TUBB6)
NM_006796.2:c.2155A>G , LRG_666t1:c.2155A>G (AFG3L2)	NP_006787.2:p.Lys719Glu
XM_011525601.1:c.1954A>G (AFG3L2)	XP_011523903.1:p.Lys652Glu
XM_011525601.3:c.1954A>G (AFG3L2)	XP_011523903.1:p.Lys652Glu
XR_002958227.1:n.451+459T>C
NM_006796.3:c.2155A>G (AFG3L2) MANE Select	NP_006787.2:p.Lys719Glu