Canonical Allele Identifier: CA2695236203
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139551222dup , CM000685.2:g.139551222dup GRCh38
NC_000023.10:g.138633381dup , CM000685.1:g.138633381dup GRCh37
NC_000023.9:g.138461047dup NCBI36
NG_007994.1:g.25487dup , LRG_556:g.25487dup

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.681dup MANE Select ENSP00000218099.2:p.Val228CysfsTer20
ENST00000643157.1:n.1348dup
ENST00000218099.6:c.681dup ENSP00000218099.2:p.Val228CysfsTer20
ENST00000394090.2:c.567dup ENSP00000377650.2:p.Val190CysfsTer20
NM_000133.3:c.681dup , LRG_556t1:c.681dup NP_000124.1:p.Val228CysfsTer20
NM_001313913.1:c.567dup NP_001300842.1:p.Val190CysfsTer20
XM_005262397.3:c.552dup XP_005262454.1:p.Val185CysfsTer20
XM_005262397.4:c.552dup XP_005262454.1:p.Val185CysfsTer20
NM_000133.4:c.681dup MANE Select NP_000124.1:p.Val228CysfsTer20
NM_001313913.2:c.567dup NP_001300842.1:p.Val190CysfsTer20