Canonical Allele Identifier: CA2695236349
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561799dup , CM000685.2:g.139561799dup GRCh38
NC_000023.10:g.138643958dup , CM000685.1:g.138643958dup GRCh37
NC_000023.9:g.138471624dup NCBI36
NG_007994.1:g.36064dup , LRG_556:g.36064dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.1114dup MANE Select ENSP00000218099.2:p.Leu372ProfsTer2
ENST00000643157.1:n.1723+58dup
ENST00000218099.6:c.1114dup ENSP00000218099.2:p.Leu372ProfsTer2
ENST00000394090.2:c.1000dup ENSP00000377650.2:p.Leu334ProfsTer2
NM_000133.3:c.1114dup , LRG_556t1:c.1114dup NP_000124.1:p.Leu372ProfsTer2
NM_001313913.1:c.1000dup NP_001300842.1:p.Leu334ProfsTer2
XM_005262397.3:c.985dup XP_005262454.1:p.Leu329ProfsTer2
XM_005262397.4:c.985dup XP_005262454.1:p.Leu329ProfsTer2
NM_000133.4:c.1114dup MANE Select NP_000124.1:p.Leu372ProfsTer2
NM_001313913.2:c.1000dup NP_001300842.1:p.Leu334ProfsTer2