Canonical Allele Identifier: CA872127783

Gene: F9

Linked Data

• dbSNP Id: rs1316814915
• MyVariant Identifiers: chrX:g.138643811_138643812insAACC (hg19) ; chrX:g.139561652_139561653insAACC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561653_139561656dup , CM000685.2:g.139561653_139561656dup	GRCh38
NC_000023.10:g.138643812_138643815dup , CM000685.1:g.138643812_138643815dup	GRCh37
NC_000023.9:g.138471478_138471481dup	NCBI36
NG_007994.1:g.35918_35921dup , LRG_556:g.35918_35921dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.968_971dup MANE Select	ENSP00000218099.2:p.Leu325ThrfsTer15
ENST00000643157.1:n.1635_1638dup
ENST00000218099.6:c.968_971dup	ENSP00000218099.2:p.Leu325ThrfsTer15
ENST00000394090.2:c.854_857dup	ENSP00000377650.2:p.Leu287ThrfsTer15
NM_000133.3:c.968_971dup , LRG_556t1:c.968_971dup	NP_000124.1:p.Leu325ThrfsTer15
NM_001313913.1:c.854_857dup	NP_001300842.1:p.Leu287ThrfsTer15
XM_005262397.3:c.839_842dup	XP_005262454.1:p.Leu282ThrfsTer15
XM_005262397.4:c.839_842dup	XP_005262454.1:p.Leu282ThrfsTer15
NM_000133.4:c.968_971dup MANE Select	NP_000124.1:p.Leu325ThrfsTer15
NM_001313913.2:c.854_857dup	NP_001300842.1:p.Leu287ThrfsTer15