Canonical Allele Identifier: CA960419809
Gene: F10 HGNC NCBI

Linked Data

gnomAD v3: 13-113149377-TG-T
gnomAD v4: 13-113149377-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113149378del , CM000675.2:g.113149378del GRCh38
NC_000013.10:g.113803692del , CM000675.1:g.113803692del GRCh37
NC_000013.9:g.112851693del NCBI36
NG_009258.1:g.31580del , LRG_548:g.31580del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.1328del MANE Select ENSP00000364709.3:p.Cys443LeufsTer24
ENST00000375551.7:c.*319del ENSP00000364701.3:n.*319del
ENST00000375559.7:c.1328del ENSP00000364709.3:p.Cys443LeufsTer24
ENST00000409306.5:c.*319del ENSP00000387092.1:n.*319del
NM_000504.3:c.1328del , LRG_548t1:c.1328del NP_000495.1:p.Cys443LeufsTer24
NM_001312674.1:c.1196del NP_001299603.1:p.Cys399LeufsTer24
NM_001312675.1:c.*319del NP_001299604.1:n.*319del
NM_000504.4:c.1328del MANE Select NP_000495.1:p.Cys443LeufsTer24
NM_001312674.2:c.1196del NP_001299603.1:p.Cys399LeufsTer24
NM_001312675.2:c.*319del NP_001299604.1:n.*319del
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