Canonical Allele Identifier: CA2448281437

Gene: TIMM8A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101348494G= , CM000685.2:g.101348494G=	GRCh38
NC_000023.10:g.100603482G= , CM000685.1:g.100603482G=	GRCh37
NC_000023.9:g.100490138G=	NCBI36
NG_009616.1:g.42731C= , LRG_128:g.42731C=
NG_011734.1:g.5476C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372902.4:c.132+39C= MANE Select	ENSP00000361993.3:n.132+39C=
ENST00000644112.2:c.132+39C=	ENSP00000494385.1:n.132+39C=
ENST00000645279.1:c.132+39C=	ENSP00000494239.1:n.132+39C=
ENST00000647480.1:n.82C=
ENST00000372902.3:c.132+39C=	ENSP00000361993.3:n.132+39C=
ENST00000480575.1:n.217+39C=
NM_001145951.1:c.132+39C=	NP_001139423.1:n.132+39C=
NM_004085.3:c.132+39C=	NP_004076.1:n.132+39C=
NM_004085.4:c.132+39C= MANE Select	NP_004076.1:n.132+39C=
NM_001145951.2:c.132+39C=	NP_001139423.1:n.132+39C=