Canonical Allele Identifier: CA2695236252

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560822_139560823del , CM000685.2:g.139560822_139560823del	GRCh38
NC_000023.10:g.138642981_138642982del , CM000685.1:g.138642981_138642982del	GRCh37
NC_000023.9:g.138470647_138470648del	NCBI36
NG_007994.1:g.35087_35088del , LRG_556:g.35087_35088del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.805_806del MANE Select	ENSP00000218099.2:p.Val269Ter
ENST00000643157.1:n.1472_1473del
ENST00000218099.6:c.805_806del	ENSP00000218099.2:p.Val269Ter
ENST00000394090.2:c.691_692del	ENSP00000377650.2:p.Val231Ter
NM_000133.3:c.805_806del , LRG_556t1:c.805_806del	NP_000124.1:p.Val269Ter
NM_001313913.1:c.691_692del	NP_001300842.1:p.Val231Ter
XM_005262397.3:c.676_677del	XP_005262454.1:p.Val226Ter
XM_005262397.4:c.676_677del	XP_005262454.1:p.Val226Ter
NM_000133.4:c.805_806del MANE Select	NP_000124.1:p.Val269Ter
NM_001313913.2:c.691_692del	NP_001300842.1:p.Val231Ter