Canonical Allele Identifier: CA2541757107

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561801_139561802del , CM000685.2:g.139561801_139561802del	GRCh38
NC_000023.10:g.138643960_138643961del , CM000685.1:g.138643960_138643961del	GRCh37
NC_000023.9:g.138471626_138471627del	NCBI36
NG_007994.1:g.36066_36067del , LRG_556:g.36066_36067del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1116_1117del MANE Select	ENSP00000218099.2:p.Arg373SerfsTer5
ENST00000643157.1:n.1723+60_1723+61del
ENST00000218099.6:c.1116_1117del	ENSP00000218099.2:p.Arg373SerfsTer5
ENST00000394090.2:c.1002_1003del	ENSP00000377650.2:p.Arg335SerfsTer5
NM_000133.3:c.1116_1117del , LRG_556t1:c.1116_1117del	NP_000124.1:p.Arg373SerfsTer5
NM_001313913.1:c.1002_1003del	NP_001300842.1:p.Arg335SerfsTer5
XM_005262397.3:c.987_988del	XP_005262454.1:p.Arg330SerfsTer5
XM_005262397.4:c.987_988del	XP_005262454.1:p.Arg330SerfsTer5
NM_000133.4:c.1116_1117del MANE Select	NP_000124.1:p.Arg373SerfsTer5
NM_001313913.2:c.1002_1003del	NP_001300842.1:p.Arg335SerfsTer5