Canonical Allele Identifier: CA2695236419

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562025_139562030delinsCATAA , CM000685.2:g.139562025_139562030delinsCATAA	GRCh38
NC_000023.10:g.138644184_138644189delinsCATAA , CM000685.1:g.138644184_138644189delinsCATAA	GRCh37
NC_000023.9:g.138471850_138471855delinsCATAA	NCBI36
NG_007994.1:g.36290_36295delinsCATAA , LRG_556:g.36290_36295delinsCATAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1340_1345delinsCATAA MANE Select	ENSP00000218099.2:p.Val447AlafsTer2
ENST00000643157.1:n.1723+284_1723+289delinsCATAA
ENST00000218099.6:c.1340_1345delinsCATAA	ENSP00000218099.2:p.Val447AlafsTer2
ENST00000394090.2:c.1226_1231delinsCATAA	ENSP00000377650.2:p.Val409AlafsTer2
NM_000133.3:c.1340_1345delinsCATAA , LRG_556t1:c.1340_1345delinsCATAA	NP_000124.1:p.Val447AlafsTer2
NM_001313913.1:c.1226_1231delinsCATAA	NP_001300842.1:p.Val409AlafsTer2
XM_005262397.3:c.1211_1216delinsCATAA	XP_005262454.1:p.Val404AlafsTer2
XM_005262397.4:c.1211_1216delinsCATAA	XP_005262454.1:p.Val404AlafsTer2
NM_000133.4:c.1340_1345delinsCATAA MANE Select	NP_000124.1:p.Val447AlafsTer2
NM_001313913.2:c.1226_1231delinsCATAA	NP_001300842.1:p.Val409AlafsTer2