Canonical Allele Identifier: CA2448281523
Gene: TIMM8A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348715T= , CM000685.2:g.101348715T= GRCh38
NC_000023.10:g.100603703T= , CM000685.1:g.100603703T= GRCh37
NC_000023.9:g.100490359T= NCBI36
NG_009616.1:g.42510A= , LRG_128:g.42510A=
NG_011734.1:g.5255A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.4:c.-51A= MANE Select ENSP00000361993.3:n.-51A=
ENST00000644112.2:c.-51A= ENSP00000494385.1:n.-51A=
ENST00000372902.3:c.-51A= ENSP00000361993.3:n.-51A=
ENST00000480575.1:n.35A=
NM_001145951.1:c.-51A= NP_001139423.1:n.-51A=
NM_004085.3:c.-51A= NP_004076.1:n.-51A=
NM_004085.4:c.-51A= MANE Select NP_004076.1:n.-51A=
NM_001145951.2:c.-51A= NP_001139423.1:n.-51A=
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