Canonical Allele Identifier: CA414444576

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138643713C>A (hg19) ; chrX:g.139561554C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561554C>A , CM000685.2:g.139561554C>A	GRCh38
NC_000023.10:g.138643713C>A , CM000685.1:g.138643713C>A	GRCh37
NC_000023.9:g.138471379C>A	NCBI36
NG_007994.1:g.35819C>A , LRG_556:g.35819C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.869C>A MANE Select	ENSP00000218099.2:p.Thr290Lys
ENST00000643157.1:n.1536C>A
ENST00000218099.6:c.869C>A	ENSP00000218099.2:p.Thr290Lys
ENST00000394090.2:c.755C>A	ENSP00000377650.2:p.Thr252Lys
NM_000133.3:c.869C>A , LRG_556t1:c.869C>A	NP_000124.1:p.Thr290Lys
NM_001313913.1:c.755C>A	NP_001300842.1:p.Thr252Lys
XM_005262397.3:c.740C>A	XP_005262454.1:p.Thr247Lys
XM_005262397.4:c.740C>A	XP_005262454.1:p.Thr247Lys
NM_000133.4:c.869C>A MANE Select	NP_000124.1:p.Thr290Lys
NM_001313913.2:c.755C>A	NP_001300842.1:p.Thr252Lys