Canonical Allele Identifier: CA2822684990
Gene: TIMM8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348459_101348460insA , CM000685.2:g.101348459_101348460insA GRCh38
NC_000023.10:g.100603447_100603448insA , CM000685.1:g.100603447_100603448insA GRCh37
NC_000023.9:g.100490103_100490104insA NCBI36
NG_009616.1:g.42765_42766insT , LRG_128:g.42765_42766insT
NG_011734.1:g.5510_5511insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.4:c.132+73_132+74insT MANE Select ENSP00000361993.3:n.132+73_132+74insT
ENST00000644112.2:c.133-59_133-58insT ENSP00000494385.1:n.133-59_133-58insT
ENST00000645279.1:c.133-59_133-58insT ENSP00000494239.1:n.133-59_133-58insT
ENST00000647480.1:n.116_117insT
ENST00000372902.3:c.132+73_132+74insT ENSP00000361993.3:n.132+73_132+74insT
ENST00000480575.1:n.218-59_218-58insT
NM_001145951.1:c.133-59_133-58insT NP_001139423.1:n.133-59_133-58insT
NM_004085.3:c.132+73_132+74insT NP_004076.1:n.132+73_132+74insT
NM_004085.4:c.132+73_132+74insT MANE Select NP_004076.1:n.132+73_132+74insT
NM_001145951.2:c.133-59_133-58insT NP_001139423.1:n.133-59_133-58insT