Canonical Allele Identifier: CA8896587

Gene: AFG3L2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12356676G>A , CM000680.2:g.12356676G>A	GRCh38
NC_000018.9:g.12356675G>A , CM000680.1:g.12356675G>A	GRCh37
NC_000018.8:g.12346675G>A	NCBI36
NG_023361.1:g.25601C>T , LRG_666:g.25601C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687337.1:c.*760+18C>T	ENSP00000508998.1:n.*760+18C>T
ENST00000688199.1:c.1026+1994C>T	ENSP00000510237.1:n.1026+1994C>T
ENST00000691179.1:c.1089+18C>T	ENSP00000509010.1:n.1089+18C>T
ENST00000691970.1:c.*541+18C>T	ENSP00000508440.1:n.*541+18C>T
ENST00000692497.1:c.1164+18C>T	ENSP00000509870.1:n.1164+18C>T
ENST00000692988.1:n.982+18C>T
ENST00000269143.8:c.1164+18C>T MANE Select	ENSP00000269143.2:n.1164+18C>T
ENST00000269143.7:c.1164+18C>T	ENSP00000269143.2:n.1164+18C>T
NM_006796.2:c.1164+18C>T , LRG_666t1:c.1164+18C>T	NP_006787.2:n.1164+18C>T
XM_011525601.1:c.1164+18C>T	XP_011523903.1:n.1164+18C>T
XM_011525601.3:c.1164+18C>T	XP_011523903.1:n.1164+18C>T
NM_006796.3:c.1164+18C>T MANE Select	NP_006787.2:n.1164+18C>T