Canonical Allele Identifier: CA2513473926

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561904_139561905insTCTTAT , CM000685.2:g.139561904_139561905insTCTTAT	GRCh38
NC_000023.10:g.138644063_138644064insTCTTAT , CM000685.1:g.138644063_138644064insTCTTAT	GRCh37
NC_000023.9:g.138471729_138471730insTCTTAT	NCBI36
NG_007994.1:g.36169_36170insTCTTAT , LRG_556:g.36169_36170insTCTTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1219_1220insTCTTAT MANE Select	ENSP00000218099.2:p.Ser406_Cys407insPheLeu
ENST00000643157.1:n.1723+163_1723+164insTCTTAT
ENST00000218099.6:c.1219_1220insTCTTAT	ENSP00000218099.2:p.Ser406_Cys407insPheLeu
ENST00000394090.2:c.1105_1106insTCTTAT	ENSP00000377650.2:p.Ser368_Cys369insPheLeu
NM_000133.3:c.1219_1220insTCTTAT , LRG_556t1:c.1219_1220insTCTTAT	NP_000124.1:p.Ser406_Cys407insPheLeu
NM_001313913.1:c.1105_1106insTCTTAT	NP_001300842.1:p.Ser368_Cys369insPheLeu
XM_005262397.3:c.1090_1091insTCTTAT	XP_005262454.1:p.Ser363_Cys364insPheLeu
XM_005262397.4:c.1090_1091insTCTTAT	XP_005262454.1:p.Ser363_Cys364insPheLeu
NM_000133.4:c.1219_1220insTCTTAT MANE Select	NP_000124.1:p.Ser406_Cys407insPheLeu
NM_001313913.2:c.1105_1106insTCTTAT	NP_001300842.1:p.Ser368_Cys369insPheLeu