Canonical Allele Identifier: CA2822685018
Gene: TIMM8A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348731_101348736dup , CM000685.2:g.101348731_101348736dup GRCh38
NC_000023.10:g.100603719_100603724dup , CM000685.1:g.100603719_100603724dup GRCh37
NC_000023.9:g.100490375_100490380dup NCBI36
NG_009616.1:g.42496_42501dup , LRG_128:g.42496_42501dup
NG_011734.1:g.5241_5246dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.4:c.-65_-60dup MANE Select ENSP00000361993.3:n.-65_-60dup
ENST00000644112.2:c.-65_-60dup ENSP00000494385.1:n.-65_-60dup
ENST00000372902.3:c.-65_-60dup ENSP00000361993.3:n.-65_-60dup
ENST00000480575.1:n.21_26dup
NM_004085.3:c.-65_-60dup NP_004076.1:n.-65_-60dup
NM_004085.4:c.-65_-60dup MANE Select NP_004076.1:n.-65_-60dup
NM_001145951.2:c.-65_-60dup NP_001139423.1:n.-65_-60dup