Canonical Allele Identifier: CA2695236338

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561772_139561790dup , CM000685.2:g.139561772_139561790dup	GRCh38
NC_000023.10:g.138643931_138643949dup , CM000685.1:g.138643931_138643949dup	GRCh37
NC_000023.9:g.138471597_138471615dup	NCBI36
NG_007994.1:g.36037_36055dup , LRG_556:g.36037_36055dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1087_1105dup MANE Select	ENSP00000218099.2:p.Leu369ArgfsTer11
ENST00000643157.1:n.1723+31_1723+49dup
ENST00000218099.6:c.1087_1105dup	ENSP00000218099.2:p.Leu369ArgfsTer11
ENST00000394090.2:c.973_991dup	ENSP00000377650.2:p.Leu331ArgfsTer11
NM_000133.3:c.1087_1105dup , LRG_556t1:c.1087_1105dup	NP_000124.1:p.Leu369ArgfsTer11
NM_001313913.1:c.973_991dup	NP_001300842.1:p.Leu331ArgfsTer11
XM_005262397.3:c.958_976dup	XP_005262454.1:p.Leu326ArgfsTer11
XM_005262397.4:c.958_976dup	XP_005262454.1:p.Leu326ArgfsTer11
NM_000133.4:c.1087_1105dup MANE Select	NP_000124.1:p.Leu369ArgfsTer11
NM_001313913.2:c.973_991dup	NP_001300842.1:p.Leu331ArgfsTer11