Canonical Allele Identifier: CA2695236261

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560853_139560854del , CM000685.2:g.139560853_139560854del	GRCh38
NC_000023.10:g.138643012_138643013del , CM000685.1:g.138643012_138643013del	GRCh37
NC_000023.9:g.138470678_138470679del	NCBI36
NG_007994.1:g.35118_35119del , LRG_556:g.35118_35119del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.836_837del MANE Select	ENSP00000218099.2:p.Ala279GlyfsTer2
ENST00000643157.1:n.1503_1504del
ENST00000218099.6:c.836_837del	ENSP00000218099.2:p.Ala279GlyfsTer2
ENST00000394090.2:c.722_723del	ENSP00000377650.2:p.Ala241GlyfsTer2
NM_000133.3:c.836_837del , LRG_556t1:c.836_837del	NP_000124.1:p.Ala279GlyfsTer2
NM_001313913.1:c.722_723del	NP_001300842.1:p.Ala241GlyfsTer2
XM_005262397.3:c.707_708del	XP_005262454.1:p.Ala236GlyfsTer2
XM_005262397.4:c.707_708del	XP_005262454.1:p.Ala236GlyfsTer2
NM_000133.4:c.836_837del MANE Select	NP_000124.1:p.Ala279GlyfsTer2
NM_001313913.2:c.722_723del	NP_001300842.1:p.Ala241GlyfsTer2