Canonical Allele Identifier: CA2461412283

Gene: F9

Linked Data

• dbSNP Id: rs1928130994

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561990_139561991del , CM000685.2:g.139561990_139561991del	GRCh38
NC_000023.10:g.138644149_138644150del , CM000685.1:g.138644149_138644150del	GRCh37
NC_000023.9:g.138471815_138471816del	NCBI36
NG_007994.1:g.36255_36256del , LRG_556:g.36255_36256del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1305_1306del MANE Select	ENSP00000218099.2:p.Ala436AsnfsTer19
ENST00000643157.1:n.1723+249_1723+250del
ENST00000218099.6:c.1305_1306del	ENSP00000218099.2:p.Ala436AsnfsTer19
ENST00000394090.2:c.1191_1192del	ENSP00000377650.2:p.Ala398AsnfsTer19
NM_000133.3:c.1305_1306del , LRG_556t1:c.1305_1306del	NP_000124.1:p.Ala436AsnfsTer19
NM_001313913.1:c.1191_1192del	NP_001300842.1:p.Ala398AsnfsTer19
XM_005262397.3:c.1176_1177del	XP_005262454.1:p.Ala393AsnfsTer19
XM_005262397.4:c.1176_1177del	XP_005262454.1:p.Ala393AsnfsTer19
NM_000133.4:c.1305_1306del MANE Select	NP_000124.1:p.Ala436AsnfsTer19
NM_001313913.2:c.1191_1192del	NP_001300842.1:p.Ala398AsnfsTer19