Canonical Allele Identifier: CA2695236185

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551124_139551125del , CM000685.2:g.139551124_139551125del	GRCh38
NC_000023.10:g.138633283_138633284del , CM000685.1:g.138633283_138633284del	GRCh37
NC_000023.9:g.138460949_138460950del	NCBI36
NG_007994.1:g.25389_25390del , LRG_556:g.25389_25390del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.583_584del MANE Select	ENSP00000218099.2:p.Val195PhefsTer3
ENST00000643157.1:n.1250_1251del
ENST00000218099.6:c.583_584del	ENSP00000218099.2:p.Val195PhefsTer3
ENST00000394090.2:c.469_470del	ENSP00000377650.2:p.Val157PhefsTer3
NM_000133.3:c.583_584del , LRG_556t1:c.583_584del	NP_000124.1:p.Val195PhefsTer3
NM_001313913.1:c.469_470del	NP_001300842.1:p.Val157PhefsTer3
XM_005262397.3:c.454_455del	XP_005262454.1:p.Val152PhefsTer3
XM_005262397.4:c.454_455del	XP_005262454.1:p.Val152PhefsTer3
NM_000133.4:c.583_584del MANE Select	NP_000124.1:p.Val195PhefsTer3
NM_001313913.2:c.469_470del	NP_001300842.1:p.Val157PhefsTer3