Canonical Allele Identifier: CA2695236396

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548467_139548476del , CM000685.2:g.139548467_139548476del	GRCh38
NC_000023.10:g.138630626_138630635del , CM000685.1:g.138630626_138630635del	GRCh37
NC_000023.9:g.138458292_138458301del	NCBI36
NG_007994.1:g.22732_22741del , LRG_556:g.22732_22741del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.496_505del MANE Select	ENSP00000218099.2:p.Asn166ProfsTer?
ENST00000643157.1:n.1163_1172del
ENST00000218099.6:c.496_505del	ENSP00000218099.2:p.Asn166ProfsTer?
ENST00000394090.2:c.382_391del	ENSP00000377650.2:p.Asn128ProfsTer?
NM_000133.3:c.496_505del , LRG_556t1:c.496_505del	NP_000124.1:p.Asn166ProfsTer?
NM_001313913.1:c.382_391del	NP_001300842.1:p.Asn128ProfsTer?
XM_005262397.3:c.392-2595_392-2586del	XP_005262454.1:n.392-2595_392-2586del
XM_005262397.4:c.392-2595_392-2586del	XP_005262454.1:n.392-2595_392-2586del
NM_000133.4:c.496_505del MANE Select	NP_000124.1:p.Asn166ProfsTer?
NM_001313913.2:c.382_391del	NP_001300842.1:p.Asn128ProfsTer?