Canonical Allele Identifier: CA2695236407

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561980del , CM000685.2:g.139561980del	GRCh38
NC_000023.10:g.138644139del , CM000685.1:g.138644139del	GRCh37
NC_000023.9:g.138471805del	NCBI36
NG_007994.1:g.36245del , LRG_556:g.36245del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1295del MANE Select	ENSP00000218099.2:p.Gly432ValfsTer6
ENST00000643157.1:n.1723+239del
ENST00000218099.6:c.1295del	ENSP00000218099.2:p.Gly432ValfsTer6
ENST00000394090.2:c.1181del	ENSP00000377650.2:p.Gly394ValfsTer6
NM_000133.3:c.1295del , LRG_556t1:c.1295del	NP_000124.1:p.Gly432ValfsTer6
NM_001313913.1:c.1181del	NP_001300842.1:p.Gly394ValfsTer6
XM_005262397.3:c.1166del	XP_005262454.1:p.Gly389ValfsTer6
XM_005262397.4:c.1166del	XP_005262454.1:p.Gly389ValfsTer6
NM_000133.4:c.1295del MANE Select	NP_000124.1:p.Gly432ValfsTer6
NM_001313913.2:c.1181del	NP_001300842.1:p.Gly394ValfsTer6