Canonical Allele Identifier: CA2461412312
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562062G= , CM000685.2:g.139562062G= GRCh38
NC_000023.10:g.138644221G= , CM000685.1:g.138644221G= GRCh37
NC_000023.9:g.138471887G= NCBI36
NG_007994.1:g.36327G= , LRG_556:g.36327G=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1377G= MANE Select ENSP00000218099.2:p.Lys459=
ENST00000643157.1:n.1723+321G=
ENST00000218099.6:c.1377G= ENSP00000218099.2:p.Lys459=
ENST00000394090.2:c.1263G= ENSP00000377650.2:p.Lys421=
NM_000133.3:c.1377G= , LRG_556t1:c.1377G= NP_000124.1:p.Lys459=
NM_001313913.1:c.1263G= NP_001300842.1:p.Lys421=
XM_005262397.3:c.1248G= XP_005262454.1:p.Lys416=
XM_005262397.4:c.1248G= XP_005262454.1:p.Lys416=
NM_000133.4:c.1377G= MANE Select NP_000124.1:p.Lys459=
NM_001313913.2:c.1263G= NP_001300842.1:p.Lys421=