Canonical Allele Identifier: CA2695236398

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561931dup , CM000685.2:g.139561931dup	GRCh38
NC_000023.10:g.138644090dup , CM000685.1:g.138644090dup	GRCh37
NC_000023.9:g.138471756dup	NCBI36
NG_007994.1:g.36196dup , LRG_556:g.36196dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1246dup MANE Select	ENSP00000218099.2:p.Val416GlyfsTer3
ENST00000643157.1:n.1723+190dup
ENST00000218099.6:c.1246dup	ENSP00000218099.2:p.Val416GlyfsTer3
ENST00000394090.2:c.1132dup	ENSP00000377650.2:p.Val378GlyfsTer3
NM_000133.3:c.1246dup , LRG_556t1:c.1246dup	NP_000124.1:p.Val416GlyfsTer3
NM_001313913.1:c.1132dup	NP_001300842.1:p.Val378GlyfsTer3
XM_005262397.3:c.1117dup	XP_005262454.1:p.Val373GlyfsTer3
XM_005262397.4:c.1117dup	XP_005262454.1:p.Val373GlyfsTer3
NM_000133.4:c.1246dup MANE Select	NP_000124.1:p.Val416GlyfsTer3
NM_001313913.2:c.1132dup	NP_001300842.1:p.Val378GlyfsTer3