Canonical Allele Identifier: CA2551094215

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562096_139562097del , CM000685.2:g.139562096_139562097del	GRCh38
NC_000023.10:g.138644255_138644256del , CM000685.1:g.138644255_138644256del	GRCh37
NC_000023.9:g.138471921_138471922del	NCBI36
NG_007994.1:g.36361_36362del , LRG_556:g.36361_36362del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.*25_*26del MANE Select	ENSP00000218099.2:n.*25_*26del
ENST00000643157.1:n.1723+355_1723+356del
ENST00000218099.6:c.*25_*26del	ENSP00000218099.2:n.*25_*26del
NM_000133.3:c.*25_*26del , LRG_556t1:c.*25_*26del	NP_000124.1:n.*25_*26del
NM_001313913.1:c.*25_*26del	NP_001300842.1:n.*25_*26del
XM_005262397.3:c.*25_*26del	XP_005262454.1:n.*25_*26del
XM_005262397.4:c.*25_*26del	XP_005262454.1:n.*25_*26del
NM_000133.4:c.*25_*26del MANE Select	NP_000124.1:n.*25_*26del
NM_001313913.2:c.*25_*26del	NP_001300842.1:n.*25_*26del