Canonical Allele Identifier: CA658640527

Gene: F9

Linked Data

• COSMIC: COSN8613386

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548273T>A , CM000685.2:g.139548273T>A	GRCh38
NC_000023.10:g.138630432T>A , CM000685.1:g.138630432T>A	GRCh37
NC_000023.9:g.138458098T>A	NCBI36
NG_007994.1:g.22538T>A , LRG_556:g.22538T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-90T>A MANE Select	ENSP00000218099.2:n.392-90T>A
ENST00000643157.1:n.1059-90T>A
ENST00000218099.6:c.392-90T>A	ENSP00000218099.2:n.392-90T>A
ENST00000394090.2:c.278-90T>A	ENSP00000377650.2:n.278-90T>A
ENST00000479617.2:n.345-90T>A
NM_000133.3:c.392-90T>A , LRG_556t1:c.392-90T>A	NP_000124.1:n.392-90T>A
NM_001313913.1:c.278-90T>A	NP_001300842.1:n.278-90T>A
XM_005262397.3:c.392-2789T>A	XP_005262454.1:n.392-2789T>A
XM_005262397.4:c.392-2789T>A	XP_005262454.1:n.392-2789T>A
NM_000133.4:c.392-90T>A MANE Select	NP_000124.1:n.392-90T>A
NM_001313913.2:c.278-90T>A	NP_001300842.1:n.278-90T>A