Canonical Allele Identifier: CA2822684998
Gene: TIMM8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348464_101348465insA , CM000685.2:g.101348464_101348465insA GRCh38
NC_000023.10:g.100603452_100603453insA , CM000685.1:g.100603452_100603453insA GRCh37
NC_000023.9:g.100490108_100490109insA NCBI36
NG_009616.1:g.42760_42761insT , LRG_128:g.42760_42761insT
NG_011734.1:g.5505_5506insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.4:c.132+68_132+69insT MANE Select ENSP00000361993.3:n.132+68_132+69insT
ENST00000644112.2:c.133-64_133-63insT ENSP00000494385.1:n.133-64_133-63insT
ENST00000645279.1:c.133-64_133-63insT ENSP00000494239.1:n.133-64_133-63insT
ENST00000647480.1:n.111_112insT
ENST00000372902.3:c.132+68_132+69insT ENSP00000361993.3:n.132+68_132+69insT
ENST00000480575.1:n.218-64_218-63insT
NM_001145951.1:c.133-64_133-63insT NP_001139423.1:n.133-64_133-63insT
NM_004085.3:c.132+68_132+69insT NP_004076.1:n.132+68_132+69insT
NM_004085.4:c.132+68_132+69insT MANE Select NP_004076.1:n.132+68_132+69insT
NM_001145951.2:c.133-64_133-63insT NP_001139423.1:n.133-64_133-63insT