Canonical Allele Identifier: CA2695236202

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551221_139551222insCAT , CM000685.2:g.139551221_139551222insCAT	GRCh38
NC_000023.10:g.138633380_138633381insCAT , CM000685.1:g.138633380_138633381insCAT	GRCh37
NC_000023.9:g.138461046_138461047insCAT	NCBI36
NG_007994.1:g.25486_25487insCAT , LRG_556:g.25486_25487insCAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.680_681insCAT MANE Select	ENSP00000218099.2:p.Val227_Val228insIle
ENST00000643157.1:n.1347_1348insCAT
ENST00000218099.6:c.680_681insCAT	ENSP00000218099.2:p.Val227_Val228insIle
ENST00000394090.2:c.566_567insCAT	ENSP00000377650.2:p.Val189_Val190insIle
NM_000133.3:c.680_681insCAT , LRG_556t1:c.680_681insCAT	NP_000124.1:p.Val227_Val228insIle
NM_001313913.1:c.566_567insCAT	NP_001300842.1:p.Val189_Val190insIle
XM_005262397.3:c.551_552insCAT	XP_005262454.1:p.Val184_Val185insIle
XM_005262397.4:c.551_552insCAT	XP_005262454.1:p.Val184_Val185insIle
NM_000133.4:c.680_681insCAT MANE Select	NP_000124.1:p.Val227_Val228insIle
NM_001313913.2:c.566_567insCAT	NP_001300842.1:p.Val189_Val190insIle