Canonical Allele Identifier: CA8896509
Community Standard Title: NM_006796.3(AFG3L2):c.1407C>T (p.Phe469=)
Gene: AFG3L2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.12351325G>A , CM000680.2:g.12351325G>A GRCh38
NC_000018.9:g.12351324G>A , CM000680.1:g.12351324G>A GRCh37
NC_000018.8:g.12341324G>A NCBI36
NG_023361.1:g.30952C>T , LRG_666:g.30952C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006796.3:c.1407C>T MANE Select NP_006787.2:p.Phe469=
ENST00000269143.8:c.1407C>T MANE Select ENSP00000269143.2:p.Phe469=
NM_006796.2:c.1407C>T , LRG_666t1:c.1407C>T NP_006787.2:p.Phe469=
ENST00000269143.7:c.1407C>T ENSP00000269143.2:p.Phe469=
ENST00000687337.1:c.*1003C>T ENSP00000508998.1:n.*1003C>T
ENST00000688199.1:c.1269C>T ENSP00000510237.1:p.Phe423=
ENST00000691179.1:c.1332C>T ENSP00000509010.1:p.Phe444=
ENST00000691970.1:c.*784C>T ENSP00000508440.1:n.*784C>T
ENST00000692497.1:c.1407C>T ENSP00000509870.1:p.Phe469=
ENST00000692988.1:n.1225C>T
XM_011525601.1:c.1407C>T XP_011523903.1:p.Phe469=
XM_011525601.3:c.1407C>T XP_011523903.1:p.Phe469=