Canonical Allele Identifier: CA2695236379

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561869del , CM000685.2:g.139561869del	GRCh38
NC_000023.10:g.138644028del , CM000685.1:g.138644028del	GRCh37
NC_000023.9:g.138471694del	NCBI36
NG_007994.1:g.36134del , LRG_556:g.36134del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1184del MANE Select	ENSP00000218099.2:p.Phe395SerfsTer?
ENST00000643157.1:n.1723+128del
ENST00000218099.6:c.1184del	ENSP00000218099.2:p.Phe395SerfsTer?
ENST00000394090.2:c.1070del	ENSP00000377650.2:p.Phe357SerfsTer?
NM_000133.3:c.1184del , LRG_556t1:c.1184del	NP_000124.1:p.Phe395SerfsTer?
NM_001313913.1:c.1070del	NP_001300842.1:p.Phe357SerfsTer?
XM_005262397.3:c.1055del	XP_005262454.1:p.Phe352SerfsTer?
XM_005262397.4:c.1055del	XP_005262454.1:p.Phe352SerfsTer?
NM_000133.4:c.1184del MANE Select	NP_000124.1:p.Phe395SerfsTer?
NM_001313913.2:c.1070del	NP_001300842.1:p.Phe357SerfsTer?