Canonical Allele Identifier: CA2695236425

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562047del , CM000685.2:g.139562047del	GRCh38
NC_000023.10:g.138644206del , CM000685.1:g.138644206del	GRCh37
NC_000023.9:g.138471872del	NCBI36
NG_007994.1:g.36312del , LRG_556:g.36312del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1362del MANE Select	ENSP00000218099.2:p.Lys455ArgfsTer28
ENST00000643157.1:n.1723+306del
ENST00000218099.6:c.1362del	ENSP00000218099.2:p.Lys455ArgfsTer28
ENST00000394090.2:c.1248del	ENSP00000377650.2:p.Lys417ArgfsTer?
NM_000133.3:c.1362del , LRG_556t1:c.1362del	NP_000124.1:p.Lys455ArgfsTer28
NM_001313913.1:c.1248del	NP_001300842.1:p.Lys417ArgfsTer28
XM_005262397.3:c.1233del	XP_005262454.1:p.Lys412ArgfsTer28
XM_005262397.4:c.1233del	XP_005262454.1:p.Lys412ArgfsTer28
NM_000133.4:c.1362del MANE Select	NP_000124.1:p.Lys455ArgfsTer28
NM_001313913.2:c.1248del	NP_001300842.1:p.Lys417ArgfsTer28