Canonical Allele Identifier: CA2461412155

Gene: F9

Linked Data

• dbSNP Id: rs1928113665

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561742_139561743del , CM000685.2:g.139561742_139561743del	GRCh38
NC_000023.10:g.138643901_138643902del , CM000685.1:g.138643901_138643902del	GRCh37
NC_000023.9:g.138471567_138471568del	NCBI36
NG_007994.1:g.36007_36008del , LRG_556:g.36007_36008del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1057_1058del MANE Select	ENSP00000218099.2:p.Val353LysfsTer20
ENST00000643157.1:n.1723+1_1723+2del
ENST00000218099.6:c.1057_1058del	ENSP00000218099.2:p.Val353LysfsTer20
ENST00000394090.2:c.943_944del	ENSP00000377650.2:p.Val315LysfsTer20
NM_000133.3:c.1057_1058del , LRG_556t1:c.1057_1058del	NP_000124.1:p.Val353LysfsTer20
NM_001313913.1:c.943_944del	NP_001300842.1:p.Val315LysfsTer20
XM_005262397.3:c.928_929del	XP_005262454.1:p.Val310LysfsTer20
XM_005262397.4:c.928_929del	XP_005262454.1:p.Val310LysfsTer20
NM_000133.4:c.1057_1058del MANE Select	NP_000124.1:p.Val353LysfsTer20
NM_001313913.2:c.943_944del	NP_001300842.1:p.Val315LysfsTer20