Canonical Allele Identifier: CA2448281459
Gene: TIMM8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348565G= , CM000685.2:g.101348565G= GRCh38
NC_000023.10:g.100603553G= , CM000685.1:g.100603553G= GRCh37
NC_000023.9:g.100490209G= NCBI36
NG_009616.1:g.42660C= , LRG_128:g.42660C=
NG_011734.1:g.5405C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372902.4:c.100C= MANE Select ENSP00000361993.3:p.Gln34=
ENST00000644112.2:c.100C= ENSP00000494385.1:p.Gln34=
ENST00000645279.1:c.100C= ENSP00000494239.1:p.Gln34=
ENST00000647480.1:n.11C=
ENST00000372902.3:c.100C= ENSP00000361993.3:p.Gln34=
ENST00000480575.1:n.185C=
NM_001145951.1:c.100C= NP_001139423.1:p.Gln34=
NM_004085.3:c.100C= NP_004076.1:p.Gln34=
NM_004085.4:c.100C= MANE Select NP_004076.1:p.Gln34=
NM_001145951.2:c.100C= NP_001139423.1:p.Gln34=