Canonical Allele Identifier: CA414443531

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560819T>A , CM000685.2:g.139560819T>A	GRCh38
NC_000023.10:g.138642978T>A , CM000685.1:g.138642978T>A	GRCh37
NC_000023.9:g.138470644T>A	NCBI36
NG_007994.1:g.35084T>A , LRG_556:g.35084T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000133.4:c.802T>A MANE Select	NP_000124.1:p.Cys268Ser
ENST00000218099.7:c.802T>A MANE Select	ENSP00000218099.2:p.Cys268Ser
NM_000133.3:c.802T>A , LRG_556t1:c.802T>A	NP_000124.1:p.Cys268Ser
NM_001313913.1:c.688T>A	NP_001300842.1:p.Cys230Ser
NM_001313913.2:c.688T>A	NP_001300842.1:p.Cys230Ser
ENST00000218099.6:c.802T>A	ENSP00000218099.2:p.Cys268Ser
ENST00000394090.2:c.688T>A	ENSP00000377650.2:p.Cys230Ser
ENST00000643157.1:n.1469T>A
XM_005262397.3:c.673T>A	XP_005262454.1:p.Cys225Ser
XM_005262397.4:c.673T>A	XP_005262454.1:p.Cys225Ser