Canonical Allele Identifier: CA2573159262

Gene: F9

Linked Data

• ClinVar Variation Id: 1439880
• ClinVar RCV Id: RCV001965414 ; RCV002271705
• dbSNP Id: rs2148361119

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548356_139548359del , CM000685.2:g.139548356_139548359del	GRCh38
NC_000023.10:g.138630515_138630518del , CM000685.1:g.138630515_138630518del	GRCh37
NC_000023.9:g.138458181_138458184del	NCBI36
NG_007994.1:g.22621_22624del , LRG_556:g.22621_22624del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-7_392-4del MANE Select	ENSP00000218099.2:n.392-7_392-4del
ENST00000643157.1:n.1059-7_1059-4del
ENST00000218099.6:c.392-7_392-4del	ENSP00000218099.2:n.392-7_392-4del
ENST00000394090.2:c.278-7_278-4del	ENSP00000377650.2:n.278-7_278-4del
ENST00000479617.2:n.345-7_345-4del
NM_000133.3:c.392-7_392-4del , LRG_556t1:c.392-7_392-4del	NP_000124.1:n.392-7_392-4del
NM_001313913.1:c.278-7_278-4del	NP_001300842.1:n.278-7_278-4del
XM_005262397.3:c.392-2706_392-2703del	XP_005262454.1:n.392-2706_392-2703del
XM_005262397.4:c.392-2706_392-2703del	XP_005262454.1:n.392-2706_392-2703del
NM_000133.4:c.392-7_392-4del MANE Select	NP_000124.1:n.392-7_392-4del
NM_001313913.2:c.278-7_278-4del	NP_001300842.1:n.278-7_278-4del