Canonical Allele Identifier: CA2695236397

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548473_139548488del , CM000685.2:g.139548473_139548488del	GRCh38
NC_000023.10:g.138630632_138630647del , CM000685.1:g.138630632_138630647del	GRCh37
NC_000023.9:g.138458298_138458313del	NCBI36
NG_007994.1:g.22738_22753del , LRG_556:g.22738_22753del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.502_517del MANE Select	ENSP00000218099.2:p.Lys168GlnfsTer30
ENST00000643157.1:n.1169_1184del
ENST00000218099.6:c.502_517del	ENSP00000218099.2:p.Lys168GlnfsTer30
ENST00000394090.2:c.388_403del	ENSP00000377650.2:p.Lys130GlnfsTer30
NM_000133.3:c.502_517del , LRG_556t1:c.502_517del	NP_000124.1:p.Lys168GlnfsTer30
NM_001313913.1:c.388_403del	NP_001300842.1:p.Lys130GlnfsTer30
XM_005262397.3:c.392-2589_392-2574del	XP_005262454.1:n.392-2589_392-2574del
XM_005262397.4:c.392-2589_392-2574del	XP_005262454.1:n.392-2589_392-2574del
NM_000133.4:c.502_517del MANE Select	NP_000124.1:p.Lys168GlnfsTer30
NM_001313913.2:c.388_403del	NP_001300842.1:p.Lys130GlnfsTer30