Canonical Allele Identifier: CA2695236212
Gene: F9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139537150del , CM000685.2:g.139537150del GRCh38
NC_000023.10:g.138619309del , CM000685.1:g.138619309del GRCh37
NC_000023.9:g.138446975del NCBI36
NG_007994.1:g.11415del , LRG_556:g.11415del

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.229del MANE Select ENSP00000218099.2:p.Val77PhefsTer27
ENST00000218099.6:c.229del ENSP00000218099.2:p.Val77PhefsTer27
ENST00000394090.2:c.229del ENSP00000377650.2:p.Val77PhefsTer18
ENST00000479617.2:n.236del
NM_000133.3:c.229del , LRG_556t1:c.229del NP_000124.1:p.Val77PhefsTer27
NM_001313913.1:c.229del NP_001300842.1:p.Val77PhefsTer18
XM_005262397.3:c.229del XP_005262454.1:p.Val77PhefsTer27
XM_005262397.4:c.229del XP_005262454.1:p.Val77PhefsTer27
NM_000133.4:c.229del MANE Select NP_000124.1:p.Val77PhefsTer27
NM_001313913.2:c.229del NP_001300842.1:p.Val77PhefsTer18
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