Canonical Allele Identifier: CA2461412270
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561959T= , CM000685.2:g.139561959T= GRCh38
NC_000023.10:g.138644118T= , CM000685.1:g.138644118T= GRCh37
NC_000023.9:g.138471784T= NCBI36
NG_007994.1:g.36224T= , LRG_556:g.36224T=

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1274T= MANE Select ENSP00000218099.2:p.Leu425=
ENST00000643157.1:n.1723+218T=
ENST00000218099.6:c.1274T= ENSP00000218099.2:p.Leu425=
ENST00000394090.2:c.1160T= ENSP00000377650.2:p.Leu387=
NM_000133.3:c.1274T= , LRG_556t1:c.1274T= NP_000124.1:p.Leu425=
NM_001313913.1:c.1160T= NP_001300842.1:p.Leu387=
XM_005262397.3:c.1145T= XP_005262454.1:p.Leu382=
XM_005262397.4:c.1145T= XP_005262454.1:p.Leu382=
NM_000133.4:c.1274T= MANE Select NP_000124.1:p.Leu425=
NM_001313913.2:c.1160T= NP_001300842.1:p.Leu387=