Canonical Allele Identifier: CA2576459019
Gene: AFG3L2 HGNC NCBI
TUBB6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.12337577T>C , CM000680.2:g.12337577T>C GRCh38
NC_000018.9:g.12337576T>C , CM000680.1:g.12337576T>C GRCh37
NC_000018.8:g.12327576T>C NCBI36
NG_023361.1:g.44700A>G , LRG_666:g.44700A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000687337.1:c.*1577-42A>G (AFG3L2) ENSP00000508998.1:n.*1577-42A>G
ENST00000687477.1:n.517-42A>G (AFG3L2)
ENST00000688199.1:c.1843-42A>G (AFG3L2) ENSP00000510237.1:n.1843-42A>G
ENST00000691179.1:c.1906-42A>G (AFG3L2) ENSP00000509010.1:n.1906-42A>G
ENST00000691970.1:c.*1358-42A>G (AFG3L2) ENSP00000508440.1:n.*1358-42A>G
ENST00000692497.1:c.*411-42A>G (AFG3L2) ENSP00000509870.1:n.*411-42A>G
ENST00000692988.1:n.1799-42A>G (AFG3L2)
ENST00000269143.8:c.1981-42A>G (AFG3L2) MANE Select ENSP00000269143.2:n.1981-42A>G
ENST00000269143.7:c.1981-42A>G (AFG3L2) ENSP00000269143.2:n.1981-42A>G
ENST00000586691.1:c.88-6472T>C (TUBB6)
NM_006796.2:c.1981-42A>G , LRG_666t1:c.1981-42A>G (AFG3L2) NP_006787.2:n.1981-42A>G
XM_011525601.1:c.1780-42A>G (AFG3L2) XP_011523903.1:n.1780-42A>G
XM_011525601.3:c.1780-42A>G (AFG3L2) XP_011523903.1:n.1780-42A>G
XR_002958227.1:n.451+675T>C
NM_006796.3:c.1981-42A>G (AFG3L2) MANE Select NP_006787.2:n.1981-42A>G