Canonical Allele Identifier: CA2285200422

Gene: AFG3L2 TUBB6

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12340230T= , CM000680.2:g.12340230T=	GRCh38
NC_000018.9:g.12340229T= , CM000680.1:g.12340229T=	GRCh37
NC_000018.8:g.12330229T=	NCBI36
NG_023361.1:g.42047A= , LRG_666:g.42047A=

Transcript Alleles

HGVS	Amino-acid Change
NM_006796.3:c.1951A= (AFG3L2) MANE Select	NP_006787.2:p.Arg651=
ENST00000269143.8:c.1951A= (AFG3L2) MANE Select	ENSP00000269143.2:p.Arg651=
NM_006796.2:c.1951A= , LRG_666t1:c.1951A= (AFG3L2)	NP_006787.2:p.Arg651=
ENST00000269143.7:c.1951A= (AFG3L2)	ENSP00000269143.2:p.Arg651=
ENST00000586691.1:c.88-3819T= (TUBB6)
ENST00000687337.1:c.*1547A= (AFG3L2)	ENSP00000508998.1:n.*1547A=
ENST00000687477.1:n.487A= (AFG3L2)
ENST00000688199.1:c.1813A= (AFG3L2)	ENSP00000510237.1:p.Arg605=
ENST00000691179.1:c.1876A= (AFG3L2)	ENSP00000509010.1:p.Arg626=
ENST00000691970.1:c.*1328A= (AFG3L2)	ENSP00000508440.1:n.*1328A=
ENST00000692497.1:c.*381A= (AFG3L2)	ENSP00000509870.1:n.*381A=
ENST00000692988.1:n.1769A= (AFG3L2)
XM_011525601.1:c.1780-2695A= (AFG3L2)	XP_011523903.1:n.1780-2695A=
XM_011525601.3:c.1780-2695A= (AFG3L2)	XP_011523903.1:n.1780-2695A=
XR_001753363.1:n.415+1650T=
XR_002958227.1:n.451+3328T=