Canonical Allele Identifier: CA658394164

Gene: TIMM8A

Linked Data

• COSMIC: COSN16128164

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101348717dup , CM000685.2:g.101348717dup	GRCh38
NC_000023.10:g.100603705dup , CM000685.1:g.100603705dup	GRCh37
NC_000023.9:g.100490361dup	NCBI36
NG_009616.1:g.42508dup , LRG_128:g.42508dup
NG_011734.1:g.5253dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372902.4:c.-53dup MANE Select	ENSP00000361993.3:n.-53dup
ENST00000644112.2:c.-53dup	ENSP00000494385.1:n.-53dup
ENST00000372902.3:c.-53dup	ENSP00000361993.3:n.-53dup
ENST00000480575.1:n.33dup
NM_001145951.1:c.-53dup	NP_001139423.1:n.-53dup
NM_004085.3:c.-53dup	NP_004076.1:n.-53dup
NM_004085.4:c.-53dup MANE Select	NP_004076.1:n.-53dup
NM_001145951.2:c.-53dup	NP_001139423.1:n.-53dup