Canonical Allele Identifier: CA414447197

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138644145A>C (hg19) ; chrX:g.139561986A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561986A>C , CM000685.2:g.139561986A>C	GRCh38
NC_000023.10:g.138644145A>C , CM000685.1:g.138644145A>C	GRCh37
NC_000023.9:g.138471811A>C	NCBI36
NG_007994.1:g.36251A>C , LRG_556:g.36251A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1301A>C MANE Select	ENSP00000218099.2:p.Glu434Ala
ENST00000643157.1:n.1723+245A>C
ENST00000218099.6:c.1301A>C	ENSP00000218099.2:p.Glu434Ala
ENST00000394090.2:c.1187A>C	ENSP00000377650.2:p.Glu396Ala
NM_000133.3:c.1301A>C , LRG_556t1:c.1301A>C	NP_000124.1:p.Glu434Ala
NM_001313913.1:c.1187A>C	NP_001300842.1:p.Glu396Ala
XM_005262397.3:c.1172A>C	XP_005262454.1:p.Glu391Ala
XM_005262397.4:c.1172A>C	XP_005262454.1:p.Glu391Ala
NM_000133.4:c.1301A>C MANE Select	NP_000124.1:p.Glu434Ala
NM_001313913.2:c.1187A>C	NP_001300842.1:p.Glu396Ala