Canonical Allele Identifier: CA2448281457
Gene: TIMM8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348560C= , CM000685.2:g.101348560C= GRCh38
NC_000023.10:g.100603548C= , CM000685.1:g.100603548C= GRCh37
NC_000023.9:g.100490204C= NCBI36
NG_009616.1:g.42665G= , LRG_128:g.42665G=
NG_011734.1:g.5410G=

Transcript Alleles

HGVS Amino-acid change
ENST00000372902.4:c.105G= MANE Select ENSP00000361993.3:p.Leu35=
ENST00000644112.2:c.105G= ENSP00000494385.1:p.Leu35=
ENST00000645279.1:c.105G= ENSP00000494239.1:p.Leu35=
ENST00000647480.1:n.16G=
ENST00000372902.3:c.105G= ENSP00000361993.3:p.Leu35=
ENST00000480575.1:n.190G=
NM_001145951.1:c.105G= NP_001139423.1:p.Leu35=
NM_004085.3:c.105G= NP_004076.1:p.Leu35=
NM_004085.4:c.105G= MANE Select NP_004076.1:p.Leu35=
NM_001145951.2:c.105G= NP_001139423.1:p.Leu35=