Canonical Allele Identifier: CA2448281456
Gene: TIMM8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348553G= , CM000685.2:g.101348553G= GRCh38
NC_000023.10:g.100603541G= , CM000685.1:g.100603541G= GRCh37
NC_000023.9:g.100490197G= NCBI36
NG_009616.1:g.42672C= , LRG_128:g.42672C=
NG_011734.1:g.5417C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372902.4:c.112C= MANE Select ENSP00000361993.3:p.Gln38=
ENST00000644112.2:c.112C= ENSP00000494385.1:p.Gln38=
ENST00000645279.1:c.112C= ENSP00000494239.1:p.Gln38=
ENST00000647480.1:n.23C=
ENST00000372902.3:c.112C= ENSP00000361993.3:p.Gln38=
ENST00000480575.1:n.197C=
NM_001145951.1:c.112C= NP_001139423.1:p.Gln38=
NM_004085.3:c.112C= NP_004076.1:p.Gln38=
NM_004085.4:c.112C= MANE Select NP_004076.1:p.Gln38=
NM_001145951.2:c.112C= NP_001139423.1:p.Gln38=