Canonical Allele Identifier: CA915951979

Gene: F9

Linked Data

• ClinVar Variation Id: 811407
• ClinVar RCV Id: RCV001001249
• dbSNP Id: rs1603267391

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561791_139561798del , CM000685.2:g.139561791_139561798del	GRCh38
NC_000023.10:g.138643950_138643957del , CM000685.1:g.138643950_138643957del	GRCh37
NC_000023.9:g.138471616_138471623del	NCBI36
NG_007994.1:g.36056_36063del , LRG_556:g.36056_36063del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1106_1113del MANE Select	ENSP00000218099.2:p.Leu369ProfsTer2
ENST00000643157.1:n.1723+50_1723+57del
ENST00000218099.6:c.1106_1113del	ENSP00000218099.2:p.Leu369ProfsTer2
ENST00000394090.2:c.992_999del	ENSP00000377650.2:p.Leu331ProfsTer2
NM_000133.3:c.1106_1113del , LRG_556t1:c.1106_1113del	NP_000124.1:p.Leu369ProfsTer2
NM_001313913.1:c.992_999del	NP_001300842.1:p.Leu331ProfsTer2
XM_005262397.3:c.977_984del	XP_005262454.1:p.Leu326ProfsTer2
XM_005262397.4:c.977_984del	XP_005262454.1:p.Leu326ProfsTer2
NM_000133.4:c.1106_1113del MANE Select	NP_000124.1:p.Leu369ProfsTer2
NM_001313913.2:c.992_999del	NP_001300842.1:p.Leu331ProfsTer2