Canonical Allele Identifier: CA414444532

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138643703A>C (hg19) ; chrX:g.139561544A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561544A>C , CM000685.2:g.139561544A>C	GRCh38
NC_000023.10:g.138643703A>C , CM000685.1:g.138643703A>C	GRCh37
NC_000023.9:g.138471369A>C	NCBI36
NG_007994.1:g.35809A>C , LRG_556:g.35809A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.859A>C MANE Select	ENSP00000218099.2:p.Thr287Pro
ENST00000643157.1:n.1526A>C
ENST00000218099.6:c.859A>C	ENSP00000218099.2:p.Thr287Pro
ENST00000394090.2:c.745A>C	ENSP00000377650.2:p.Thr249Pro
NM_000133.3:c.859A>C , LRG_556t1:c.859A>C	NP_000124.1:p.Thr287Pro
NM_001313913.1:c.745A>C	NP_001300842.1:p.Thr249Pro
XM_005262397.3:c.730A>C	XP_005262454.1:p.Thr244Pro
XM_005262397.4:c.730A>C	XP_005262454.1:p.Thr244Pro
NM_000133.4:c.859A>C MANE Select	NP_000124.1:p.Thr287Pro
NM_001313913.2:c.745A>C	NP_001300842.1:p.Thr249Pro