Canonical Allele Identifier: CA2695236283

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561592_139561594del , CM000685.2:g.139561592_139561594del	GRCh38
NC_000023.10:g.138643751_138643753del , CM000685.1:g.138643751_138643753del	GRCh37
NC_000023.9:g.138471417_138471419del	NCBI36
NG_007994.1:g.35857_35859del , LRG_556:g.35857_35859del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.907_909del MANE Select	ENSP00000218099.2:p.His303del
ENST00000643157.1:n.1574_1576del
ENST00000218099.6:c.907_909del	ENSP00000218099.2:p.His303del
ENST00000394090.2:c.793_795del	ENSP00000377650.2:p.His265del
NM_000133.3:c.907_909del , LRG_556t1:c.907_909del	NP_000124.1:p.His303del
NM_001313913.1:c.793_795del	NP_001300842.1:p.His265del
XM_005262397.3:c.778_780del	XP_005262454.1:p.His260del
XM_005262397.4:c.778_780del	XP_005262454.1:p.His260del
NM_000133.4:c.907_909del MANE Select	NP_000124.1:p.His303del
NM_001313913.2:c.793_795del	NP_001300842.1:p.His265del