Canonical Allele Identifier: CA2285198899

Gene: AFG3L2 TUBB6

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337451A= , CM000680.2:g.12337451A=	GRCh38
NC_000018.9:g.12337450A= , CM000680.1:g.12337450A=	GRCh37
NC_000018.8:g.12327450A=	NCBI36
NG_023361.1:g.44826T= , LRG_666:g.44826T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687337.1:c.*1661T= (AFG3L2)	ENSP00000508998.1:n.*1661T=
ENST00000687477.1:n.601T= (AFG3L2)
ENST00000688199.1:c.1927T= (AFG3L2)	ENSP00000510237.1:p.Tyr643=
ENST00000691179.1:c.1990T= (AFG3L2)	ENSP00000509010.1:p.Tyr664=
ENST00000691970.1:c.*1442T= (AFG3L2)	ENSP00000508440.1:n.*1442T=
ENST00000692497.1:c.*495T= (AFG3L2)	ENSP00000509870.1:n.*495T=
ENST00000692988.1:n.1883T= (AFG3L2)
ENST00000269143.8:c.2065T= (AFG3L2) MANE Select	ENSP00000269143.2:p.Tyr689=
ENST00000269143.7:c.2065T= (AFG3L2)	ENSP00000269143.2:p.Tyr689=
ENST00000586691.1:c.88-6598A= (TUBB6)
NM_006796.2:c.2065T= , LRG_666t1:c.2065T= (AFG3L2)	NP_006787.2:p.Tyr689=
XM_011525601.1:c.1864T= (AFG3L2)	XP_011523903.1:p.Tyr622=
XM_011525601.3:c.1864T= (AFG3L2)	XP_011523903.1:p.Tyr622=
XR_002958227.1:n.451+549A=
NM_006796.3:c.2065T= (AFG3L2) MANE Select	NP_006787.2:p.Tyr689=