Canonical Allele Identifier: CA2695236349

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561799dup , CM000685.2:g.139561799dup	GRCh38
NC_000023.10:g.138643958dup , CM000685.1:g.138643958dup	GRCh37
NC_000023.9:g.138471624dup	NCBI36
NG_007994.1:g.36064dup , LRG_556:g.36064dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1114dup MANE Select	ENSP00000218099.2:p.Leu372ProfsTer2
ENST00000643157.1:n.1723+58dup
ENST00000218099.6:c.1114dup	ENSP00000218099.2:p.Leu372ProfsTer2
ENST00000394090.2:c.1000dup	ENSP00000377650.2:p.Leu334ProfsTer2
NM_000133.3:c.1114dup , LRG_556t1:c.1114dup	NP_000124.1:p.Leu372ProfsTer2
NM_001313913.1:c.1000dup	NP_001300842.1:p.Leu334ProfsTer2
XM_005262397.3:c.985dup	XP_005262454.1:p.Leu329ProfsTer2
XM_005262397.4:c.985dup	XP_005262454.1:p.Leu329ProfsTer2
NM_000133.4:c.1114dup MANE Select	NP_000124.1:p.Leu372ProfsTer2
NM_001313913.2:c.1000dup	NP_001300842.1:p.Leu334ProfsTer2