Canonical Allele Identifier: CA2461412156

Gene: F9

Linked Data

• dbSNP Id: rs1928113797

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561744_139561747dup , CM000685.2:g.139561744_139561747dup	GRCh38
NC_000023.10:g.138643903_138643906dup , CM000685.1:g.138643903_138643906dup	GRCh37
NC_000023.9:g.138471569_138471572dup	NCBI36
NG_007994.1:g.36009_36012dup , LRG_556:g.36009_36012dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1059_1062dup MANE Select	ENSP00000218099.2:p.Gly355LysfsTer20
ENST00000643157.1:n.1723+3_1723+6dup
ENST00000218099.6:c.1059_1062dup	ENSP00000218099.2:p.Gly355LysfsTer20
ENST00000394090.2:c.945_948dup	ENSP00000377650.2:p.Gly317LysfsTer20
NM_000133.3:c.1059_1062dup , LRG_556t1:c.1059_1062dup	NP_000124.1:p.Gly355LysfsTer20
NM_001313913.1:c.945_948dup	NP_001300842.1:p.Gly317LysfsTer20
XM_005262397.3:c.930_933dup	XP_005262454.1:p.Gly312LysfsTer20
XM_005262397.4:c.930_933dup	XP_005262454.1:p.Gly312LysfsTer20
NM_000133.4:c.1059_1062dup MANE Select	NP_000124.1:p.Gly355LysfsTer20
NM_001313913.2:c.945_948dup	NP_001300842.1:p.Gly317LysfsTer20