Canonical Allele Identifier: CA2461412246

Gene: F9

Linked Data

• dbSNP Id: rs1928126315

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561928del , CM000685.2:g.139561928del	GRCh38
NC_000023.10:g.138644087del , CM000685.1:g.138644087del	GRCh37
NC_000023.9:g.138471753del	NCBI36
NG_007994.1:g.36193del , LRG_556:g.36193del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1243del MANE Select	ENSP00000218099.2:p.His415MetfsTer11
ENST00000643157.1:n.1723+187del
ENST00000218099.6:c.1243del	ENSP00000218099.2:p.His415MetfsTer11
ENST00000394090.2:c.1129del	ENSP00000377650.2:p.His377MetfsTer11
NM_000133.3:c.1243del , LRG_556t1:c.1243del	NP_000124.1:p.His415MetfsTer11
NM_001313913.1:c.1129del	NP_001300842.1:p.His377MetfsTer11
XM_005262397.3:c.1114del	XP_005262454.1:p.His372MetfsTer11
XM_005262397.4:c.1114del	XP_005262454.1:p.His372MetfsTer11
NM_000133.4:c.1243del MANE Select	NP_000124.1:p.His415MetfsTer11
NM_001313913.2:c.1129del	NP_001300842.1:p.His377MetfsTer11