Canonical Allele Identifier: CA2695236348

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548366del , CM000685.2:g.139548366del	GRCh38
NC_000023.10:g.138630525del , CM000685.1:g.138630525del	GRCh37
NC_000023.9:g.138458191del	NCBI36
NG_007994.1:g.22631del , LRG_556:g.22631del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.395del MANE Select	ENSP00000218099.2:p.Val132GlufsTer?
ENST00000643157.1:n.1062del
ENST00000218099.6:c.395del	ENSP00000218099.2:p.Val132GlufsTer?
ENST00000394090.2:c.281del	ENSP00000377650.2:p.Val94GlufsTer?
ENST00000479617.2:n.348del
NM_000133.3:c.395del , LRG_556t1:c.395del	NP_000124.1:p.Val132GlufsTer?
NM_001313913.1:c.281del	NP_001300842.1:p.Val94GlufsTer?
XM_005262397.3:c.392-2696del	XP_005262454.1:n.392-2696del
XM_005262397.4:c.392-2696del	XP_005262454.1:n.392-2696del
NM_000133.4:c.395del MANE Select	NP_000124.1:p.Val132GlufsTer?
NM_001313913.2:c.281del	NP_001300842.1:p.Val94GlufsTer?