Canonical Allele Identifier: CA2448281423
Gene: TIMM8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348457G= , CM000685.2:g.101348457G= GRCh38
NC_000023.10:g.100603445G= , CM000685.1:g.100603445G= GRCh37
NC_000023.9:g.100490101G= NCBI36
NG_009616.1:g.42768C= , LRG_128:g.42768C=
NG_011734.1:g.5513C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372902.4:c.132+76C= MANE Select ENSP00000361993.3:n.132+76C=
ENST00000644112.2:c.133-56C= ENSP00000494385.1:n.133-56C=
ENST00000645279.1:c.133-56C= ENSP00000494239.1:n.133-56C=
ENST00000647480.1:n.119C=
ENST00000372902.3:c.132+76C= ENSP00000361993.3:n.132+76C=
ENST00000480575.1:n.218-56C=
NM_001145951.1:c.133-56C= NP_001139423.1:n.133-56C=
NM_004085.3:c.132+76C= NP_004076.1:n.132+76C=
NM_004085.4:c.132+76C= MANE Select NP_004076.1:n.132+76C=
NM_001145951.2:c.133-56C= NP_001139423.1:n.133-56C=