Canonical Allele Identifier: CA2695236422

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562032del , CM000685.2:g.139562032del	GRCh38
NC_000023.10:g.138644191del , CM000685.1:g.138644191del	GRCh37
NC_000023.9:g.138471857del	NCBI36
NG_007994.1:g.36297del , LRG_556:g.36297del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1347del MANE Select	ENSP00000218099.2:p.Tyr450MetfsTer?
ENST00000643157.1:n.1723+291del
ENST00000218099.6:c.1347del	ENSP00000218099.2:p.Tyr450MetfsTer?
ENST00000394090.2:c.1233del	ENSP00000377650.2:p.Tyr412MetfsTer?
NM_000133.3:c.1347del , LRG_556t1:c.1347del	NP_000124.1:p.Tyr450MetfsTer?
NM_001313913.1:c.1233del	NP_001300842.1:p.Tyr412MetfsTer?
XM_005262397.3:c.1218del	XP_005262454.1:p.Tyr407MetfsTer?
XM_005262397.4:c.1218del	XP_005262454.1:p.Tyr407MetfsTer?
NM_000133.4:c.1347del MANE Select	NP_000124.1:p.Tyr450MetfsTer?
NM_001313913.2:c.1233del	NP_001300842.1:p.Tyr412MetfsTer?