Canonical Allele Identifier: CA401951510
Community Standard Title: NM_006796.3(AFG3L2):c.1586C>T (p.Ala529Val)
Gene: AFG3L2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.12348350G>A , CM000680.2:g.12348350G>A GRCh38
NC_000018.9:g.12348349G>A , CM000680.1:g.12348349G>A GRCh37
NC_000018.8:g.12338349G>A NCBI36
NG_023361.1:g.33927C>T , LRG_666:g.33927C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006796.3:c.1586C>T MANE Select NP_006787.2:p.Ala529Val
ENST00000269143.8:c.1586C>T MANE Select ENSP00000269143.2:p.Ala529Val
NM_006796.2:c.1586C>T , LRG_666t1:c.1586C>T NP_006787.2:p.Ala529Val
ENST00000269143.7:c.1586C>T ENSP00000269143.2:p.Ala529Val
ENST00000687337.1:c.*1182C>T ENSP00000508998.1:n.*1182C>T
ENST00000688199.1:c.1448C>T ENSP00000510237.1:p.Ala483Val
ENST00000691179.1:c.1511C>T ENSP00000509010.1:p.Ala504Val
ENST00000691970.1:c.*963C>T ENSP00000508440.1:n.*963C>T
ENST00000692497.1:c.1586C>T ENSP00000509870.1:p.Ala529Val
ENST00000692988.1:n.1404C>T
XM_011525601.1:c.1586C>T XP_011523903.1:p.Ala529Val
XM_011525601.3:c.1586C>T XP_011523903.1:p.Ala529Val