Canonical Allele Identifier: CA2579663792
Gene: TIMM8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348709del , CM000685.2:g.101348709del GRCh38
NC_000023.10:g.100603697del , CM000685.1:g.100603697del GRCh37
NC_000023.9:g.100490353del NCBI36
NG_009616.1:g.42516del , LRG_128:g.42516del
NG_011734.1:g.5261del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.4:c.-45del MANE Select ENSP00000361993.3:n.-45del
ENST00000644112.2:c.-45del ENSP00000494385.1:n.-45del
ENST00000372902.3:c.-45del ENSP00000361993.3:n.-45del
ENST00000480575.1:n.41del
NM_001145951.1:c.-45del NP_001139423.1:n.-45del
NM_004085.3:c.-45del NP_004076.1:n.-45del
NM_004085.4:c.-45del MANE Select NP_004076.1:n.-45del
NM_001145951.2:c.-45del NP_001139423.1:n.-45del