Canonical Allele Identifier: CA2461408624

Gene: F9

Linked Data

• dbSNP Id: rs1927834124

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551180_139551181del , CM000685.2:g.139551180_139551181del	GRCh38
NC_000023.10:g.138633339_138633340del , CM000685.1:g.138633339_138633340del	GRCh37
NC_000023.9:g.138461005_138461006del	NCBI36
NG_007994.1:g.25445_25446del , LRG_556:g.25445_25446del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.639_640del MANE Select	ENSP00000218099.2:p.Ile214HisfsTer8
ENST00000643157.1:n.1306_1307del
ENST00000218099.6:c.639_640del	ENSP00000218099.2:p.Ile214HisfsTer8
ENST00000394090.2:c.525_526del	ENSP00000377650.2:p.Ile176HisfsTer8
NM_000133.3:c.639_640del , LRG_556t1:c.639_640del	NP_000124.1:p.Ile214HisfsTer8
NM_001313913.1:c.525_526del	NP_001300842.1:p.Ile176HisfsTer8
XM_005262397.3:c.510_511del	XP_005262454.1:p.Ile171HisfsTer8
XM_005262397.4:c.510_511del	XP_005262454.1:p.Ile171HisfsTer8
NM_000133.4:c.639_640del MANE Select	NP_000124.1:p.Ile214HisfsTer8
NM_001313913.2:c.525_526del	NP_001300842.1:p.Ile176HisfsTer8