Canonical Allele Identifier: CA2695236205

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551225dup , CM000685.2:g.139551225dup	GRCh38
NC_000023.10:g.138633384dup , CM000685.1:g.138633384dup	GRCh37
NC_000023.9:g.138461050dup	NCBI36
NG_007994.1:g.25490dup , LRG_556:g.25490dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.684dup MANE Select	ENSP00000218099.2:p.Gly229TrpfsTer19
ENST00000643157.1:n.1351dup
ENST00000218099.6:c.684dup	ENSP00000218099.2:p.Gly229TrpfsTer19
ENST00000394090.2:c.570dup	ENSP00000377650.2:p.Gly191TrpfsTer19
NM_000133.3:c.684dup , LRG_556t1:c.684dup	NP_000124.1:p.Gly229TrpfsTer19
NM_001313913.1:c.570dup	NP_001300842.1:p.Gly191TrpfsTer19
XM_005262397.3:c.555dup	XP_005262454.1:p.Gly186TrpfsTer19
XM_005262397.4:c.555dup	XP_005262454.1:p.Gly186TrpfsTer19
NM_000133.4:c.684dup MANE Select	NP_000124.1:p.Gly229TrpfsTer19
NM_001313913.2:c.570dup	NP_001300842.1:p.Gly191TrpfsTer19