Canonical Allele Identifier: CA413916077
Gene: TIMM8A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348598T>A , CM000685.2:g.101348598T>A GRCh38
NC_000023.10:g.100603586T>A , CM000685.1:g.100603586T>A GRCh37
NC_000023.9:g.100490242T>A NCBI36
NG_009616.1:g.42627A>T , LRG_128:g.42627A>T
NG_011734.1:g.5372A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.4:c.67A>T MANE Select ENSP00000361993.3:p.Ile23Phe
ENST00000644112.2:c.67A>T ENSP00000494385.1:p.Ile23Phe
ENST00000645279.1:c.67A>T ENSP00000494239.1:p.Ile23Phe
ENST00000372902.3:c.67A>T ENSP00000361993.3:p.Ile23Phe
ENST00000480575.1:n.152A>T
NM_001145951.1:c.67A>T NP_001139423.1:p.Ile23Phe
NM_004085.3:c.67A>T NP_004076.1:p.Ile23Phe
NM_004085.4:c.67A>T MANE Select NP_004076.1:p.Ile23Phe
NM_001145951.2:c.67A>T NP_001139423.1:p.Ile23Phe