Canonical Allele Identifier: CA2285198962

Gene: AFG3L2 TUBB6

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337519A= , CM000680.2:g.12337519A=	GRCh38
NC_000018.9:g.12337518A= , CM000680.1:g.12337518A=	GRCh37
NC_000018.8:g.12327518A=	NCBI36
NG_023361.1:g.44758T= , LRG_666:g.44758T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000687337.1:c.*1593T= (AFG3L2)	ENSP00000508998.1:n.*1593T=
ENST00000687477.1:n.533T= (AFG3L2)
ENST00000688199.1:c.1859T= (AFG3L2)	ENSP00000510237.1:p.Met620=
ENST00000691179.1:c.1922T= (AFG3L2)	ENSP00000509010.1:p.Met641=
ENST00000691970.1:c.*1374T= (AFG3L2)	ENSP00000508440.1:n.*1374T=
ENST00000692497.1:c.*427T= (AFG3L2)	ENSP00000509870.1:n.*427T=
ENST00000692988.1:n.1815T= (AFG3L2)
ENST00000269143.8:c.1997T= (AFG3L2) MANE Select	ENSP00000269143.2:p.Met666=
ENST00000269143.7:c.1997T= (AFG3L2)	ENSP00000269143.2:p.Met666=
ENST00000586691.1:c.88-6530A= (TUBB6)
NM_006796.2:c.1997T= , LRG_666t1:c.1997T= (AFG3L2)	NP_006787.2:p.Met666=
XM_011525601.1:c.1796T= (AFG3L2)	XP_011523903.1:p.Met599=
XM_011525601.3:c.1796T= (AFG3L2)	XP_011523903.1:p.Met599=
XR_002958227.1:n.451+617A=
NM_006796.3:c.1997T= (AFG3L2) MANE Select	NP_006787.2:p.Met666=