Canonical Allele Identifier: CA2448281526
Gene: TIMM8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348733A= , CM000685.2:g.101348733A= GRCh38
NC_000023.10:g.100603721A= , CM000685.1:g.100603721A= GRCh37
NC_000023.9:g.100490377A= NCBI36
NG_009616.1:g.42492T= , LRG_128:g.42492T=
NG_011734.1:g.5237T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.4:c.-69T= MANE Select ENSP00000361993.3:n.-69T=
ENST00000644112.2:c.-69T= ENSP00000494385.1:n.-69T=
ENST00000372902.3:c.-69T= ENSP00000361993.3:n.-69T=
ENST00000480575.1:n.17T=
NM_004085.3:c.-69T= NP_004076.1:n.-69T=
NM_004085.4:c.-69T= MANE Select NP_004076.1:n.-69T=
NM_001145951.2:c.-69T= NP_001139423.1:n.-69T=