Canonical Allele Identifier: CA2285198944
Gene: AFG3L2 HGNC NCBI
TUBB6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.12337497G= , CM000680.2:g.12337497G= GRCh38
NC_000018.9:g.12337496G= , CM000680.1:g.12337496G= GRCh37
NC_000018.8:g.12327496G= NCBI36
NG_023361.1:g.44780C= , LRG_666:g.44780C=

Transcript Alleles

HGVS Amino-acid change
ENST00000687337.1:c.*1615C= (AFG3L2) ENSP00000508998.1:n.*1615C=
ENST00000687477.1:n.555C= (AFG3L2)
ENST00000688199.1:c.1881C= (AFG3L2) ENSP00000510237.1:p.Ile627=
ENST00000691179.1:c.1944C= (AFG3L2) ENSP00000509010.1:p.Ile648=
ENST00000691970.1:c.*1396C= (AFG3L2) ENSP00000508440.1:n.*1396C=
ENST00000692497.1:c.*449C= (AFG3L2) ENSP00000509870.1:n.*449C=
ENST00000692988.1:n.1837C= (AFG3L2)
ENST00000269143.8:c.2019C= (AFG3L2) MANE Select ENSP00000269143.2:p.Ile673=
ENST00000269143.7:c.2019C= (AFG3L2) ENSP00000269143.2:p.Ile673=
ENST00000586691.1:c.88-6552G= (TUBB6)
NM_006796.2:c.2019C= , LRG_666t1:c.2019C= (AFG3L2) NP_006787.2:p.Ile673=
XM_011525601.1:c.1818C= (AFG3L2) XP_011523903.1:p.Ile606=
XM_011525601.3:c.1818C= (AFG3L2) XP_011523903.1:p.Ile606=
XR_002958227.1:n.451+595G=
NM_006796.3:c.2019C= (AFG3L2) MANE Select NP_006787.2:p.Ile673=