Canonical Allele Identifier: CA2461412308
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562050G= , CM000685.2:g.139562050G= GRCh38
NC_000023.10:g.138644209G= , CM000685.1:g.138644209G= GRCh37
NC_000023.9:g.138471875G= NCBI36
NG_007994.1:g.36315G= , LRG_556:g.36315G=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1365G= MANE Select ENSP00000218099.2:p.Lys455=
ENST00000643157.1:n.1723+309G=
ENST00000218099.6:c.1365G= ENSP00000218099.2:p.Lys455=
ENST00000394090.2:c.1251G= ENSP00000377650.2:p.Lys417=
NM_000133.3:c.1365G= , LRG_556t1:c.1365G= NP_000124.1:p.Lys455=
NM_001313913.1:c.1251G= NP_001300842.1:p.Lys417=
XM_005262397.3:c.1236G= XP_005262454.1:p.Lys412=
XM_005262397.4:c.1236G= XP_005262454.1:p.Lys412=
NM_000133.4:c.1365G= MANE Select NP_000124.1:p.Lys455=
NM_001313913.2:c.1251G= NP_001300842.1:p.Lys417=