Canonical Allele Identifier: CA2448281507
Gene: TIMM8A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348697C= , CM000685.2:g.101348697C= GRCh38
NC_000023.10:g.100603685C= , CM000685.1:g.100603685C= GRCh37
NC_000023.9:g.100490341C= NCBI36
NG_009616.1:g.42528G= , LRG_128:g.42528G=
NG_011734.1:g.5273G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.4:c.-33G= MANE Select ENSP00000361993.3:n.-33G=
ENST00000644112.2:c.-33G= ENSP00000494385.1:n.-33G=
ENST00000372902.3:c.-33G= ENSP00000361993.3:n.-33G=
ENST00000480575.1:n.53G=
NM_001145951.1:c.-33G= NP_001139423.1:n.-33G=
NM_004085.3:c.-33G= NP_004076.1:n.-33G=
NM_004085.4:c.-33G= MANE Select NP_004076.1:n.-33G=
NM_001145951.2:c.-33G= NP_001139423.1:n.-33G=
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