Canonical Allele Identifier: CA8896680

Gene: AFG3L2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12359961G>A , CM000680.2:g.12359961G>A	GRCh38
NC_000018.9:g.12359960G>A , CM000680.1:g.12359960G>A	GRCh37
NC_000018.8:g.12349960G>A	NCBI36
NG_023361.1:g.22316C>T , LRG_666:g.22316C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006796.3:c.718C>T MANE Select	NP_006787.2:p.Arg240Trp
ENST00000269143.8:c.718C>T MANE Select	ENSP00000269143.2:p.Arg240Trp
NM_006796.2:c.718C>T , LRG_666t1:c.718C>T	NP_006787.2:p.Arg240Trp
ENST00000269143.7:c.718C>T	ENSP00000269143.2:p.Arg240Trp
ENST00000590811.1:c.353C>T
ENST00000591848.1:n.273C>T
ENST00000687337.1:c.*314C>T	ENSP00000508998.1:n.*314C>T
ENST00000688199.1:c.718C>T	ENSP00000510237.1:p.Arg240Trp
ENST00000691179.1:c.643C>T	ENSP00000509010.1:p.Arg215Trp
ENST00000691970.1:c.*95C>T	ENSP00000508440.1:n.*95C>T
ENST00000692497.1:c.718C>T	ENSP00000509870.1:p.Arg240Trp
ENST00000692988.1:n.536C>T
XM_011525601.1:c.718C>T	XP_011523903.1:p.Arg240Trp
XM_011525601.3:c.718C>T	XP_011523903.1:p.Arg240Trp