Canonical Allele Identifier: CA413915492
Gene: TIMM8A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348561A>G , CM000685.2:g.101348561A>G GRCh38
NC_000023.10:g.100603549A>G , CM000685.1:g.100603549A>G GRCh37
NC_000023.9:g.100490205A>G NCBI36
NG_009616.1:g.42664T>C , LRG_128:g.42664T>C
NG_011734.1:g.5409T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372902.4:c.104T>C MANE Select ENSP00000361993.3:p.Leu35Pro
ENST00000644112.2:c.104T>C ENSP00000494385.1:p.Leu35Pro
ENST00000645279.1:c.104T>C ENSP00000494239.1:p.Leu35Pro
ENST00000647480.1:n.15T>C
ENST00000372902.3:c.104T>C ENSP00000361993.3:p.Leu35Pro
ENST00000480575.1:n.189T>C
NM_001145951.1:c.104T>C NP_001139423.1:p.Leu35Pro
NM_004085.3:c.104T>C NP_004076.1:p.Leu35Pro
NM_004085.4:c.104T>C MANE Select NP_004076.1:p.Leu35Pro
NM_001145951.2:c.104T>C NP_001139423.1:p.Leu35Pro