Canonical Allele Identifier: CA2823819893

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548266dup , CM000685.2:g.139548266dup	GRCh38
NC_000023.10:g.138630425dup , CM000685.1:g.138630425dup	GRCh37
NC_000023.9:g.138458091dup	NCBI36
NG_007994.1:g.22531dup , LRG_556:g.22531dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-97dup MANE Select	ENSP00000218099.2:n.392-97dup
ENST00000643157.1:n.1059-97dup
ENST00000218099.6:c.392-97dup	ENSP00000218099.2:n.392-97dup
ENST00000394090.2:c.278-97dup	ENSP00000377650.2:n.278-97dup
ENST00000479617.2:n.345-97dup
NM_000133.3:c.392-97dup , LRG_556t1:c.392-97dup	NP_000124.1:n.392-97dup
NM_001313913.1:c.278-97dup	NP_001300842.1:n.278-97dup
XM_005262397.3:c.392-2796dup	XP_005262454.1:n.392-2796dup
XM_005262397.4:c.392-2796dup	XP_005262454.1:n.392-2796dup
NM_000133.4:c.392-97dup MANE Select	NP_000124.1:n.392-97dup
NM_001313913.2:c.278-97dup	NP_001300842.1:n.278-97dup