Canonical Allele Identifier: CA414439171

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548442T>A , CM000685.2:g.139548442T>A	GRCh38
NC_000023.10:g.138630601T>A , CM000685.1:g.138630601T>A	GRCh37
NC_000023.9:g.138458267T>A	NCBI36
NG_007994.1:g.22707T>A , LRG_556:g.22707T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.471T>A MANE Select	ENSP00000218099.2:p.Cys157Ter
ENST00000643157.1:n.1138T>A
ENST00000218099.6:c.471T>A	ENSP00000218099.2:p.Cys157Ter
ENST00000394090.2:c.357T>A	ENSP00000377650.2:p.Cys119Ter
NM_000133.3:c.471T>A , LRG_556t1:c.471T>A	NP_000124.1:p.Cys157Ter
NM_001313913.1:c.357T>A	NP_001300842.1:p.Cys119Ter
XM_005262397.3:c.392-2620T>A	XP_005262454.1:n.392-2620T>A
XM_005262397.4:c.392-2620T>A	XP_005262454.1:n.392-2620T>A
NM_000133.4:c.471T>A MANE Select	NP_000124.1:p.Cys157Ter
NM_001313913.2:c.357T>A	NP_001300842.1:p.Cys119Ter