Canonical Allele Identifier: CA413916472
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1555976416

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348633C>T , CM000685.2:g.101348633C>T GRCh38
NC_000023.10:g.100603621C>T , CM000685.1:g.100603621C>T GRCh37
NC_000023.9:g.100490277C>T NCBI36
NG_009616.1:g.42592G>A , LRG_128:g.42592G>A
NG_011734.1:g.5337G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.4:c.32G>A MANE Select ENSP00000361993.3:p.Gly11Asp
ENST00000644112.2:c.32G>A ENSP00000494385.1:p.Gly11Asp
ENST00000645279.1:c.32G>A ENSP00000494239.1:p.Gly11Asp
ENST00000372902.3:c.32G>A ENSP00000361993.3:p.Gly11Asp
ENST00000480575.1:n.117G>A
NM_001145951.1:c.32G>A NP_001139423.1:p.Gly11Asp
NM_004085.3:c.32G>A NP_004076.1:p.Gly11Asp
NM_004085.4:c.32G>A MANE Select NP_004076.1:p.Gly11Asp
NM_001145951.2:c.32G>A NP_001139423.1:p.Gly11Asp