Canonical Allele Identifier: CA2500895716

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537120_139537121del , CM000685.2:g.139537120_139537121del	GRCh38
NC_000023.10:g.138619279_138619280del , CM000685.1:g.138619279_138619280del	GRCh37
NC_000023.9:g.138446945_138446946del	NCBI36
NG_007994.1:g.11385_11386del , LRG_556:g.11385_11386del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.199_200del MANE Select	ENSP00000218099.2:p.Glu67LysfsTer3
ENST00000218099.6:c.199_200del	ENSP00000218099.2:p.Glu67LysfsTer3
ENST00000394090.2:c.199_200del	ENSP00000377650.2:p.Glu67LysfsTer3
ENST00000479617.2:n.206_207del
NM_000133.3:c.199_200del , LRG_556t1:c.199_200del	NP_000124.1:p.Glu67LysfsTer3
NM_001313913.1:c.199_200del	NP_001300842.1:p.Glu67LysfsTer3
XM_005262397.3:c.199_200del	XP_005262454.1:p.Glu67LysfsTer3
XM_005262397.4:c.199_200del	XP_005262454.1:p.Glu67LysfsTer3
NM_000133.4:c.199_200del MANE Select	NP_000124.1:p.Glu67LysfsTer3
NM_001313913.2:c.199_200del	NP_001300842.1:p.Glu67LysfsTer3