Canonical Allele Identifier: CA401953160
Community Standard Title: NM_006796.3(AFG3L2):c.1119T>A (p.Ser373Arg)
Gene: AFG3L2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.12356739A>T , CM000680.2:g.12356739A>T GRCh38
NC_000018.9:g.12356738A>T , CM000680.1:g.12356738A>T GRCh37
NC_000018.8:g.12346738A>T NCBI36
NG_023361.1:g.25538T>A , LRG_666:g.25538T>A

Transcript Alleles

HGVS Amino-acid Change
NM_006796.3:c.1119T>A MANE Select NP_006787.2:p.Ser373Arg
ENST00000269143.8:c.1119T>A MANE Select ENSP00000269143.2:p.Ser373Arg
NM_006796.2:c.1119T>A , LRG_666t1:c.1119T>A NP_006787.2:p.Ser373Arg
ENST00000269143.7:c.1119T>A ENSP00000269143.2:p.Ser373Arg
ENST00000687337.1:c.*715T>A ENSP00000508998.1:n.*715T>A
ENST00000688199.1:c.1026+1931T>A ENSP00000510237.1:n.1026+1931T>A
ENST00000691179.1:c.1044T>A ENSP00000509010.1:p.Ser348Arg
ENST00000691970.1:c.*496T>A ENSP00000508440.1:n.*496T>A
ENST00000692497.1:c.1119T>A ENSP00000509870.1:p.Ser373Arg
ENST00000692988.1:n.937T>A
XM_011525601.1:c.1119T>A XP_011523903.1:p.Ser373Arg
XM_011525601.3:c.1119T>A XP_011523903.1:p.Ser373Arg