Canonical Allele Identifier: CA414447189

Gene: F9

Linked Data

• dbSNP Id: rs1450707631
• gnomAD v4: X-139561985-G-A
• MyVariant Identifiers: chrX:g.138644144G>A (hg19) ; chrX:g.139561985G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561985G>A , CM000685.2:g.139561985G>A	GRCh38
NC_000023.10:g.138644144G>A , CM000685.1:g.138644144G>A	GRCh37
NC_000023.9:g.138471810G>A	NCBI36
NG_007994.1:g.36250G>A , LRG_556:g.36250G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1300G>A MANE Select	ENSP00000218099.2:p.Glu434Lys
ENST00000643157.1:n.1723+244G>A
ENST00000218099.6:c.1300G>A	ENSP00000218099.2:p.Glu434Lys
ENST00000394090.2:c.1186G>A	ENSP00000377650.2:p.Glu396Lys
NM_000133.3:c.1300G>A , LRG_556t1:c.1300G>A	NP_000124.1:p.Glu434Lys
NM_001313913.1:c.1186G>A	NP_001300842.1:p.Glu396Lys
XM_005262397.3:c.1171G>A	XP_005262454.1:p.Glu391Lys
XM_005262397.4:c.1171G>A	XP_005262454.1:p.Glu391Lys
NM_000133.4:c.1300G>A MANE Select	NP_000124.1:p.Glu434Lys
NM_001313913.2:c.1186G>A	NP_001300842.1:p.Glu396Lys