Canonical Allele Identifier: CA413916650
Gene: TIMM8A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348659A>T , CM000685.2:g.101348659A>T GRCh38
NC_000023.10:g.100603647A>T , CM000685.1:g.100603647A>T GRCh37
NC_000023.9:g.100490303A>T NCBI36
NG_009616.1:g.42566T>A , LRG_128:g.42566T>A
NG_011734.1:g.5311T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.4:c.6T>A MANE Select ENSP00000361993.3:p.Asp2Glu
ENST00000644112.2:c.6T>A ENSP00000494385.1:p.Asp2Glu
ENST00000645279.1:c.6T>A ENSP00000494239.1:p.Asp2Glu
ENST00000372902.3:c.6T>A ENSP00000361993.3:p.Asp2Glu
ENST00000480575.1:n.91T>A
NM_001145951.1:c.6T>A NP_001139423.1:p.Asp2Glu
NM_004085.3:c.6T>A NP_004076.1:p.Asp2Glu
NM_004085.4:c.6T>A MANE Select NP_004076.1:p.Asp2Glu
NM_001145951.2:c.6T>A NP_001139423.1:p.Asp2Glu