Canonical Allele Identifier: CA2461412075

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561552_139561554delinsTAC , CM000685.2:g.139561552_139561554delinsTAC	GRCh38
NC_000023.10:g.138643711_138643713delinsTAC , CM000685.1:g.138643711_138643713delinsTAC	GRCh37
NC_000023.9:g.138471377_138471379delinsTAC	NCBI36
NG_007994.1:g.35817_35819delinsTAC , LRG_556:g.35817_35819delinsTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.867_869delinsTAC MANE Select	ENSP00000218099.2:p.His289=
ENST00000643157.1:n.1534_1536delinsTAC
ENST00000218099.6:c.867_869delinsTAC	ENSP00000218099.2:p.His289=
ENST00000394090.2:c.753_755delinsTAC	ENSP00000377650.2:p.His251=
NM_000133.3:c.867_869delinsTAC , LRG_556t1:c.867_869delinsTAC	NP_000124.1:p.His289=
NM_001313913.1:c.753_755delinsTAC	NP_001300842.1:p.His251=
XM_005262397.3:c.738_740delinsTAC	XP_005262454.1:p.His246=
XM_005262397.4:c.738_740delinsTAC	XP_005262454.1:p.His246=
NM_000133.4:c.867_869delinsTAC MANE Select	NP_000124.1:p.His289=
NM_001313913.2:c.753_755delinsTAC	NP_001300842.1:p.His251=