Canonical Allele Identifier: CA2695236276

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561554del , CM000685.2:g.139561554del	GRCh38
NC_000023.10:g.138643713del , CM000685.1:g.138643713del	GRCh37
NC_000023.9:g.138471379del	NCBI36
NG_007994.1:g.35819del , LRG_556:g.35819del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.869del MANE Select	ENSP00000218099.2:p.Thr290LysfsTer7
ENST00000643157.1:n.1536del
ENST00000218099.6:c.869del	ENSP00000218099.2:p.Thr290LysfsTer7
ENST00000394090.2:c.755del	ENSP00000377650.2:p.Thr252LysfsTer7
NM_000133.3:c.869del , LRG_556t1:c.869del	NP_000124.1:p.Thr290LysfsTer7
NM_001313913.1:c.755del	NP_001300842.1:p.Thr252LysfsTer7
XM_005262397.3:c.740del	XP_005262454.1:p.Thr247LysfsTer7
XM_005262397.4:c.740del	XP_005262454.1:p.Thr247LysfsTer7
NM_000133.4:c.869del MANE Select	NP_000124.1:p.Thr290LysfsTer7
NM_001313913.2:c.755del	NP_001300842.1:p.Thr252LysfsTer7