Canonical Allele Identifier: CA2448281513
Gene: TIMM8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348700A= , CM000685.2:g.101348700A= GRCh38
NC_000023.10:g.100603688A= , CM000685.1:g.100603688A= GRCh37
NC_000023.9:g.100490344A= NCBI36
NG_009616.1:g.42525T= , LRG_128:g.42525T=
NG_011734.1:g.5270T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.4:c.-36T= MANE Select ENSP00000361993.3:n.-36T=
ENST00000644112.2:c.-36T= ENSP00000494385.1:n.-36T=
ENST00000372902.3:c.-36T= ENSP00000361993.3:n.-36T=
ENST00000480575.1:n.50T=
NM_001145951.1:c.-36T= NP_001139423.1:n.-36T=
NM_004085.3:c.-36T= NP_004076.1:n.-36T=
NM_004085.4:c.-36T= MANE Select NP_004076.1:n.-36T=
NM_001145951.2:c.-36T= NP_001139423.1:n.-36T=