Canonical Allele Identifier: CA2694293096
Gene: TIMM8A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348425_101348426insCGGGGGGGGGGGGGGTG , CM000685.2:g.101348425_101348426insCGGGGGGGGGGGGGGTG GRCh38
NC_000023.10:g.100603413_100603414insCGGGGGGGGGGGGGGTG , CM000685.1:g.100603413_100603414insCGGGGGGGGGGGGGGTG GRCh37
NC_000023.9:g.100490069_100490070insCGGGGGGGGGGGGGGTG NCBI36
NG_009616.1:g.42799_42800insCACCCCCCCCCCCCCCG , LRG_128:g.42799_42800insCACCCCCCCCCCCCCCG
NG_011734.1:g.5544_5545insCACCCCCCCCCCCCCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.4:c.132+107_132+108insCACCCCCCCCCCCCCCG MANE Select ENSP00000361993.3:n.132+107_132+108insCACCCCCCCCCCCCCCG
ENST00000644112.2:c.133-25_133-24insCACCCCCCCCCCCCCCG ENSP00000494385.1:n.133-25_133-24insCACCCCCCCCCCCCCCG
ENST00000645279.1:c.133-25_133-24insCACCCCCCCCCCCCCCG ENSP00000494239.1:n.133-25_133-24insCACCCCCCCCCCCCCCG
ENST00000647480.1:n.150_151insCACCCCCCCCCCCCCCG
ENST00000372902.3:c.132+107_132+108insCACCCCCCCCCCCCCCG ENSP00000361993.3:n.132+107_132+108insCACCCCCCCCCCCCCCG
ENST00000480575.1:n.218-25_218-24insCACCCCCCCCCCCCCCG
NM_001145951.1:c.133-25_133-24insCACCCCCCCCCCCCCCG NP_001139423.1:n.133-25_133-24insCACCCCCCCCCCCCCCG
NM_004085.3:c.132+107_132+108insCACCCCCCCCCCCCCCG NP_004076.1:n.132+107_132+108insCACCCCCCCCCCCCCCG
NM_004085.4:c.132+107_132+108insCACCCCCCCCCCCCCCG MANE Select NP_004076.1:n.132+107_132+108insCACCCCCCCCCCCCCCG
NM_001145951.2:c.133-25_133-24insCACCCCCCCCCCCCCCG NP_001139423.1:n.133-25_133-24insCACCCCCCCCCCCCCCG