Canonical Allele Identifier: CA2695236198

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551198_139551201dup , CM000685.2:g.139551198_139551201dup	GRCh38
NC_000023.10:g.138633357_138633360dup , CM000685.1:g.138633357_138633360dup	GRCh37
NC_000023.9:g.138461023_138461026dup	NCBI36
NG_007994.1:g.25463_25466dup , LRG_556:g.25463_25466dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.657_660dup MANE Select	ENSP00000218099.2:p.Phe221IlefsTer3
ENST00000643157.1:n.1324_1327dup
ENST00000218099.6:c.657_660dup	ENSP00000218099.2:p.Phe221IlefsTer3
ENST00000394090.2:c.543_546dup	ENSP00000377650.2:p.Phe183IlefsTer3
NM_000133.3:c.657_660dup , LRG_556t1:c.657_660dup	NP_000124.1:p.Phe221IlefsTer3
NM_001313913.1:c.543_546dup	NP_001300842.1:p.Phe183IlefsTer3
XM_005262397.3:c.528_531dup	XP_005262454.1:p.Phe178IlefsTer3
XM_005262397.4:c.528_531dup	XP_005262454.1:p.Phe178IlefsTer3
NM_000133.4:c.657_660dup MANE Select	NP_000124.1:p.Phe221IlefsTer3
NM_001313913.2:c.543_546dup	NP_001300842.1:p.Phe183IlefsTer3