Canonical Allele Identifier: CA645610451

Gene: F9

Linked Data

• COSMIC: COSM5455938

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551100dup , CM000685.2:g.139551100dup	GRCh38
NC_000023.10:g.138633259dup , CM000685.1:g.138633259dup	GRCh37
NC_000023.9:g.138460925dup	NCBI36
NG_007994.1:g.25365dup , LRG_556:g.25365dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.559dup MANE Select	ENSP00000218099.2:p.Ser187PhefsTer2
ENST00000643157.1:n.1226dup
ENST00000218099.6:c.559dup	ENSP00000218099.2:p.Ser187PhefsTer2
ENST00000394090.2:c.445dup	ENSP00000377650.2:p.Ser149PhefsTer2
NM_000133.3:c.559dup , LRG_556t1:c.559dup	NP_000124.1:p.Ser187PhefsTer2
NM_001313913.1:c.445dup	NP_001300842.1:p.Ser149PhefsTer2
XM_005262397.3:c.430dup	XP_005262454.1:p.Ser144PhefsTer2
XM_005262397.4:c.430dup	XP_005262454.1:p.Ser144PhefsTer2
NM_000133.4:c.559dup MANE Select	NP_000124.1:p.Ser187PhefsTer2
NM_001313913.2:c.445dup	NP_001300842.1:p.Ser149PhefsTer2