Canonical Allele Identifier: CA2579663704
Gene: TIMM8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348192del , CM000685.2:g.101348192del GRCh38
NC_000023.10:g.100603180del , CM000685.1:g.100603180del GRCh37
NC_000023.9:g.100489836del NCBI36
NG_009616.1:g.43034del , LRG_128:g.43034del
NG_011734.1:g.5779del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.4:c.132+342del MANE Select ENSP00000361993.3:n.132+342del
ENST00000644112.2:c.*196del ENSP00000494385.1:n.*196del
ENST00000645279.1:c.*196del ENSP00000494239.1:n.*196del
ENST00000647480.1:n.385del
ENST00000372902.3:c.132+342del ENSP00000361993.3:n.132+342del
ENST00000480575.1:n.428del
NM_001145951.1:c.*196del NP_001139423.1:n.*196del
NM_004085.3:c.132+342del NP_004076.1:n.132+342del
NM_004085.4:c.132+342del MANE Select NP_004076.1:n.132+342del
NM_001145951.2:c.*196del NP_001139423.1:n.*196del