Canonical Allele Identifier: CA2448281422
Gene: TIMM8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348454G= , CM000685.2:g.101348454G= GRCh38
NC_000023.10:g.100603442G= , CM000685.1:g.100603442G= GRCh37
NC_000023.9:g.100490098G= NCBI36
NG_009616.1:g.42771C= , LRG_128:g.42771C=
NG_011734.1:g.5516C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372902.4:c.132+79C= MANE Select ENSP00000361993.3:n.132+79C=
ENST00000644112.2:c.133-53C= ENSP00000494385.1:n.133-53C=
ENST00000645279.1:c.133-53C= ENSP00000494239.1:n.133-53C=
ENST00000647480.1:n.122C=
ENST00000372902.3:c.132+79C= ENSP00000361993.3:n.132+79C=
ENST00000480575.1:n.218-53C=
NM_001145951.1:c.133-53C= NP_001139423.1:n.133-53C=
NM_004085.3:c.132+79C= NP_004076.1:n.132+79C=
NM_004085.4:c.132+79C= MANE Select NP_004076.1:n.132+79C=
NM_001145951.2:c.133-53C= NP_001139423.1:n.133-53C=