Canonical Allele Identifier: CA7060471
Gene: F10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113140947C>T , CM000675.2:g.113140947C>T GRCh38
NC_000013.10:g.113795261C>T , CM000675.1:g.113795261C>T GRCh37
NC_000013.9:g.112843262C>T NCBI36
NG_009258.1:g.23149C>T , LRG_548:g.23149C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.399C>T MANE Select ENSP00000364709.3:p.Asn133=
ENST00000375551.7:c.399C>T ENSP00000364701.3:p.Asn133=
ENST00000375559.7:c.399C>T ENSP00000364709.3:p.Asn133=
ENST00000409306.5:c.399C>T ENSP00000387092.1:p.Asn133=
ENST00000410083.6:c.*358C>T ENSP00000386320.2:n.*358C>T
ENST00000477269.5:n.436C>T
ENST00000498455.1:n.428C>T
NM_000504.3:c.399C>T , LRG_548t1:c.399C>T NP_000495.1:p.Asn133=
NM_001312674.1:c.370+1477C>T NP_001299603.1:n.370+1477C>T
NM_001312675.1:c.399C>T NP_001299604.1:p.Asn133=
NM_000504.4:c.399C>T MANE Select NP_000495.1:p.Asn133=
NM_001312674.2:c.370+1477C>T NP_001299603.1:n.370+1477C>T
NM_001312675.2:c.399C>T NP_001299604.1:p.Asn133=
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