Canonical Allele Identifier: CA2695236213

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537154_139537155del , CM000685.2:g.139537154_139537155del	GRCh38
NC_000023.10:g.138619313_138619314del , CM000685.1:g.138619313_138619314del	GRCh37
NC_000023.9:g.138446979_138446980del	NCBI36
NG_007994.1:g.11419_11420del , LRG_556:g.11419_11420del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.233_234del MANE Select	ENSP00000218099.2:p.Phe78Ter
ENST00000218099.6:c.233_234del	ENSP00000218099.2:p.Phe78Ter
ENST00000394090.2:c.233_234del	ENSP00000377650.2:p.Phe78Ter
ENST00000479617.2:n.240_241del
NM_000133.3:c.233_234del , LRG_556t1:c.233_234del	NP_000124.1:p.Phe78Ter
NM_001313913.1:c.233_234del	NP_001300842.1:p.Phe78Ter
XM_005262397.3:c.233_234del	XP_005262454.1:p.Phe78Ter
XM_005262397.4:c.233_234del	XP_005262454.1:p.Phe78Ter
NM_000133.4:c.233_234del MANE Select	NP_000124.1:p.Phe78Ter
NM_001313913.2:c.233_234del	NP_001300842.1:p.Phe78Ter