Canonical Allele Identifier: CA2695236421

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562029_139562030delinsAAGGTACCAA , CM000685.2:g.139562029_139562030delinsAAGGTACCAA	GRCh38
NC_000023.10:g.138644188_138644189delinsAAGGTACCAA , CM000685.1:g.138644188_138644189delinsAAGGTACCAA	GRCh37
NC_000023.9:g.138471854_138471855delinsAAGGTACCAA	NCBI36
NG_007994.1:g.36294_36295delinsAAGGTACCAA , LRG_556:g.36294_36295delinsAAGGTACCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1344_1345delinsAAGGTACCAA MANE Select	ENSP00000218099.2:p.Val451GlnfsTer?
ENST00000643157.1:n.1723+288_1723+289delinsAAGGTACCAA
ENST00000218099.6:c.1344_1345delinsAAGGTACCAA	ENSP00000218099.2:p.Val451GlnfsTer?
ENST00000394090.2:c.1230_1231delinsAAGGTACCAA	ENSP00000377650.2:p.Val413GlnfsTer?
NM_000133.3:c.1344_1345delinsAAGGTACCAA , LRG_556t1:c.1344_1345delinsAAGGTACCAA	NP_000124.1:p.Val451GlnfsTer?
NM_001313913.1:c.1230_1231delinsAAGGTACCAA	NP_001300842.1:p.Val413GlnfsTer?
XM_005262397.3:c.1215_1216delinsAAGGTACCAA	XP_005262454.1:p.Val408GlnfsTer?
XM_005262397.4:c.1215_1216delinsAAGGTACCAA	XP_005262454.1:p.Val408GlnfsTer?
NM_000133.4:c.1344_1345delinsAAGGTACCAA MANE Select	NP_000124.1:p.Val451GlnfsTer?
NM_001313913.2:c.1230_1231delinsAAGGTACCAA	NP_001300842.1:p.Val413GlnfsTer?