Canonical Allele Identifier: CA658820747
Gene: F10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113122925_113129612del , CM000675.2:g.113122925_113129612del GRCh38
NC_000013.10:g.113777239_113783926del , CM000675.1:g.113777239_113783926del GRCh37
NC_000013.9:g.112825240_112831927del NCBI36
NG_009258.1:g.5127_11814del , LRG_548:g.5127_11814del

Transcript Alleles

HGVS Amino-acid change
ENST00000375559.8:c.70_231del
ENST00000375551.7:c.70_231del
ENST00000375559.7:c.70_231del
ENST00000409306.5:c.70_231del
ENST00000410083.6:c.70_231del
ENST00000477269.5:n.107_268del
ENST00000483537.1:n.90_251del
NM_000504.3:c.70_231del , LRG_548t1:c.70_231del
NM_001312674.1:c.70_231del
NM_001312675.1:c.70_231del
NM_000504.4:c.70_231del
NM_001312674.2:c.70_231del
NM_001312675.2:c.70_231del
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