Canonical Allele Identifier: CA2695236356

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561830_139561831del , CM000685.2:g.139561830_139561831del	GRCh38
NC_000023.10:g.138643989_138643990del , CM000685.1:g.138643989_138643990del	GRCh37
NC_000023.9:g.138471655_138471656del	NCBI36
NG_007994.1:g.36095_36096del , LRG_556:g.36095_36096del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1145_1146del MANE Select	ENSP00000218099.2:p.Cys382SerfsTer10
ENST00000643157.1:n.1723+89_1723+90del
ENST00000218099.6:c.1145_1146del	ENSP00000218099.2:p.Cys382SerfsTer10
ENST00000394090.2:c.1031_1032del	ENSP00000377650.2:p.Cys344SerfsTer10
NM_000133.3:c.1145_1146del , LRG_556t1:c.1145_1146del	NP_000124.1:p.Cys382SerfsTer10
NM_001313913.1:c.1031_1032del	NP_001300842.1:p.Cys344SerfsTer10
XM_005262397.3:c.1016_1017del	XP_005262454.1:p.Cys339SerfsTer10
XM_005262397.4:c.1016_1017del	XP_005262454.1:p.Cys339SerfsTer10
NM_000133.4:c.1145_1146del MANE Select	NP_000124.1:p.Cys382SerfsTer10
NM_001313913.2:c.1031_1032del	NP_001300842.1:p.Cys344SerfsTer10