Canonical Allele Identifier: CA658820950

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541120dup , CM000685.2:g.139541120dup	GRCh38
NC_000023.10:g.138623279dup , CM000685.1:g.138623279dup	GRCh37
NC_000023.9:g.138450945dup	NCBI36
NG_007994.1:g.15385dup , LRG_556:g.15385dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.322dup MANE Select	ENSP00000218099.2:p.Cys108LeufsTer4
ENST00000218099.6:c.322dup	ENSP00000218099.2:p.Cys108LeufsTer4
ENST00000394090.2:c.277+3734dup	ENSP00000377650.2:n.277+3734dup
ENST00000479617.2:n.275dup
NM_000133.3:c.322dup , LRG_556t1:c.322dup	NP_000124.1:p.Cys108LeufsTer4
NM_001313913.1:c.277+3734dup	NP_001300842.1:n.277+3734dup
XM_005262397.3:c.322dup	XP_005262454.1:p.Cys108LeufsTer4
XM_005262397.4:c.322dup	XP_005262454.1:p.Cys108LeufsTer4
NM_000133.4:c.322dup MANE Select	NP_000124.1:p.Cys108LeufsTer4
NM_001313913.2:c.277+3734dup	NP_001300842.1:n.277+3734dup