Canonical Allele Identifier: CA2448281428
Gene: TIMM8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348470C= , CM000685.2:g.101348470C= GRCh38
NC_000023.10:g.100603458C= , CM000685.1:g.100603458C= GRCh37
NC_000023.9:g.100490114C= NCBI36
NG_009616.1:g.42755G= , LRG_128:g.42755G=
NG_011734.1:g.5500G=

Transcript Alleles

HGVS Amino-acid change
ENST00000372902.4:c.132+63G= MANE Select ENSP00000361993.3:n.132+63G=
ENST00000644112.2:c.132+63G= ENSP00000494385.1:n.132+63G=
ENST00000645279.1:c.132+63G= ENSP00000494239.1:n.132+63G=
ENST00000647480.1:n.106G=
ENST00000372902.3:c.132+63G= ENSP00000361993.3:n.132+63G=
ENST00000480575.1:n.217+63G=
NM_001145951.1:c.132+63G= NP_001139423.1:n.132+63G=
NM_004085.3:c.132+63G= NP_004076.1:n.132+63G=
NM_004085.4:c.132+63G= MANE Select NP_004076.1:n.132+63G=
NM_001145951.2:c.132+63G= NP_001139423.1:n.132+63G=