Canonical Allele Identifier: CA869301843
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1184477415
gnomAD v4: X-101348773-ACTGCGTCGGCGCGAGGCAGGCGTCCAACTCCACCCCGCCGC-A
MyVariant Identifiers: chrX:g.101348774_101348814del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348776_101348816del , CM000685.2:g.101348776_101348816del GRCh38
NC_000023.10:g.100603764_100603804del , CM000685.1:g.100603764_100603804del GRCh37
NC_000023.9:g.100490420_100490460del NCBI36
NG_009616.1:g.42411_42451del , LRG_128:g.42411_42451del
NG_011734.1:g.5156_5196del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-150_-110del ENSP00000361993.3:n.-150_-110del
NM_004085.3:c.-150_-110del NP_004076.1:n.-150_-110del
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