Canonical Allele Identifier: CA2694839866
Gene: F9 HGNC NCBI

Linked Data

gnomAD v4: X-139561449-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561452del , CM000685.2:g.139561452del GRCh38
NC_000023.10:g.138643611del , CM000685.1:g.138643611del GRCh37
NC_000023.9:g.138471277del NCBI36
NG_007994.1:g.35717del , LRG_556:g.35717del

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.839-72del MANE Select ENSP00000218099.2:n.839-72del
ENST00000643157.1:n.1506-72del
ENST00000218099.6:c.839-72del ENSP00000218099.2:n.839-72del
ENST00000394090.2:c.725-72del ENSP00000377650.2:n.725-72del
NM_000133.3:c.839-72del , LRG_556t1:c.839-72del NP_000124.1:n.839-72del
NM_001313913.1:c.725-72del NP_001300842.1:n.725-72del
XM_005262397.3:c.710-72del XP_005262454.1:n.710-72del
XM_005262397.4:c.710-72del XP_005262454.1:n.710-72del
NM_000133.4:c.839-72del MANE Select NP_000124.1:n.839-72del
NM_001313913.2:c.725-72del NP_001300842.1:n.725-72del
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