Canonical Allele Identifier: CA8896507

Gene: AFG3L2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12351297T>A , CM000680.2:g.12351297T>A	GRCh38
NC_000018.9:g.12351296T>A , CM000680.1:g.12351296T>A	GRCh37
NC_000018.8:g.12341296T>A	NCBI36
NG_023361.1:g.30980A>T , LRG_666:g.30980A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006796.3:c.1426+9A>T MANE Select	NP_006787.2:n.1426+9A>T
ENST00000269143.8:c.1426+9A>T MANE Select	ENSP00000269143.2:n.1426+9A>T
NM_006796.2:c.1426+9A>T , LRG_666t1:c.1426+9A>T	NP_006787.2:n.1426+9A>T
ENST00000269143.7:c.1426+9A>T	ENSP00000269143.2:n.1426+9A>T
ENST00000687337.1:c.*1022+9A>T	ENSP00000508998.1:n.*1022+9A>T
ENST00000688199.1:c.1288+9A>T	ENSP00000510237.1:n.1288+9A>T
ENST00000691179.1:c.1351+9A>T	ENSP00000509010.1:n.1351+9A>T
ENST00000691970.1:c.*803+9A>T	ENSP00000508440.1:n.*803+9A>T
ENST00000692497.1:c.1426+9A>T	ENSP00000509870.1:n.1426+9A>T
ENST00000692988.1:n.1244+9A>T
XM_011525601.1:c.1426+9A>T	XP_011523903.1:n.1426+9A>T
XM_011525601.3:c.1426+9A>T	XP_011523903.1:n.1426+9A>T