Canonical Allele Identifier: CA2461412253

Gene: F9

Linked Data

• dbSNP Id: rs1928127010

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561932_139561937del , CM000685.2:g.139561932_139561937del	GRCh38
NC_000023.10:g.138644091_138644096del , CM000685.1:g.138644091_138644096del	GRCh37
NC_000023.9:g.138471757_138471762del	NCBI36
NG_007994.1:g.36197_36202del , LRG_556:g.36197_36202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1247_1252del MANE Select	ENSP00000218099.2:p.Val416_Thr417del
ENST00000643157.1:n.1723+191_1723+196del
ENST00000218099.6:c.1247_1252del	ENSP00000218099.2:p.Val416_Thr417del
ENST00000394090.2:c.1133_1138del	ENSP00000377650.2:p.Val378_Thr379del
NM_000133.3:c.1247_1252del , LRG_556t1:c.1247_1252del	NP_000124.1:p.Val416_Thr417del
NM_001313913.1:c.1133_1138del	NP_001300842.1:p.Val378_Thr379del
XM_005262397.3:c.1118_1123del	XP_005262454.1:p.Val373_Thr374del
XM_005262397.4:c.1118_1123del	XP_005262454.1:p.Val373_Thr374del
NM_000133.4:c.1247_1252del MANE Select	NP_000124.1:p.Val416_Thr417del
NM_001313913.2:c.1133_1138del	NP_001300842.1:p.Val378_Thr379del