Canonical Allele Identifier: CA414445121

Gene: F9

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561659T>G , CM000685.2:g.139561659T>G	GRCh38
NC_000023.10:g.138643818T>G , CM000685.1:g.138643818T>G	GRCh37
NC_000023.9:g.138471484T>G	NCBI36
NG_007994.1:g.35924T>G , LRG_556:g.35924T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.974T>G MANE Select	ENSP00000218099.2:p.Leu325Ter
ENST00000643157.1:n.1641T>G
ENST00000218099.6:c.974T>G	ENSP00000218099.2:p.Leu325Ter
ENST00000394090.2:c.860T>G	ENSP00000377650.2:p.Leu287Ter
NM_000133.3:c.974T>G , LRG_556t1:c.974T>G	NP_000124.1:p.Leu325Ter
NM_001313913.1:c.860T>G	NP_001300842.1:p.Leu287Ter
XM_005262397.3:c.845T>G	XP_005262454.1:p.Leu282Ter
XM_005262397.4:c.845T>G	XP_005262454.1:p.Leu282Ter
NM_000133.4:c.974T>G MANE Select	NP_000124.1:p.Leu325Ter
NM_001313913.2:c.860T>G	NP_001300842.1:p.Leu287Ter