Canonical Allele Identifier: CA872127669

Gene: F9

Linked Data

• dbSNP Id: rs1174937062
• MyVariant Identifiers: chrX:g.138643759_138643760insA (hg19) ; chrX:g.139561600_139561601insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561602dup , CM000685.2:g.139561602dup	GRCh38
NC_000023.10:g.138643761dup , CM000685.1:g.138643761dup	GRCh37
NC_000023.9:g.138471427dup	NCBI36
NG_007994.1:g.35867dup , LRG_556:g.35867dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.917dup MANE Select	ENSP00000218099.2:p.Asn306LysfsTer5
ENST00000643157.1:n.1584dup
ENST00000218099.6:c.917dup	ENSP00000218099.2:p.Asn306LysfsTer5
ENST00000394090.2:c.803dup	ENSP00000377650.2:p.Asn268LysfsTer5
NM_000133.3:c.917dup , LRG_556t1:c.917dup	NP_000124.1:p.Asn306LysfsTer5
NM_001313913.1:c.803dup	NP_001300842.1:p.Asn268LysfsTer5
XM_005262397.3:c.788dup	XP_005262454.1:p.Asn263LysfsTer5
XM_005262397.4:c.788dup	XP_005262454.1:p.Asn263LysfsTer5
NM_000133.4:c.917dup MANE Select	NP_000124.1:p.Asn306LysfsTer5
NM_001313913.2:c.803dup	NP_001300842.1:p.Asn268LysfsTer5