Canonical Allele Identifier: CA2448281329

Gene: TIMM8A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101348175T= , CM000685.2:g.101348175T=	GRCh38
NC_000023.10:g.100603163T= , CM000685.1:g.100603163T=	GRCh37
NC_000023.9:g.100489819T=	NCBI36
NG_009616.1:g.43050A= , LRG_128:g.43050A=
NG_011734.1:g.5795A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372902.4:c.132+358A= MANE Select	ENSP00000361993.3:n.132+358A=
ENST00000644112.2:c.*212A=	ENSP00000494385.1:n.*212A=
ENST00000645279.1:c.*212A=	ENSP00000494239.1:n.*212A=
ENST00000647480.1:n.401A=
ENST00000372902.3:c.132+358A=	ENSP00000361993.3:n.132+358A=
ENST00000480575.1:n.444A=
NM_001145951.1:c.*212A=	NP_001139423.1:n.*212A=
NM_004085.3:c.132+358A=	NP_004076.1:n.132+358A=
NM_004085.4:c.132+358A= MANE Select	NP_004076.1:n.132+358A=
NM_001145951.2:c.*212A=	NP_001139423.1:n.*212A=