Canonical Allele Identifier: CA2695236280

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561563del , CM000685.2:g.139561563del	GRCh38
NC_000023.10:g.138643722del , CM000685.1:g.138643722del	GRCh37
NC_000023.9:g.138471388del	NCBI36
NG_007994.1:g.35828del , LRG_556:g.35828del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.878del MANE Select	ENSP00000218099.2:p.Lys293SerfsTer4
ENST00000643157.1:n.1545del
ENST00000218099.6:c.878del	ENSP00000218099.2:p.Lys293SerfsTer4
ENST00000394090.2:c.764del	ENSP00000377650.2:p.Lys255SerfsTer4
NM_000133.3:c.878del , LRG_556t1:c.878del	NP_000124.1:p.Lys293SerfsTer4
NM_001313913.1:c.764del	NP_001300842.1:p.Lys255SerfsTer4
XM_005262397.3:c.749del	XP_005262454.1:p.Lys250SerfsTer4
XM_005262397.4:c.749del	XP_005262454.1:p.Lys250SerfsTer4
NM_000133.4:c.878del MANE Select	NP_000124.1:p.Lys293SerfsTer4
NM_001313913.2:c.764del	NP_001300842.1:p.Lys255SerfsTer4