Canonical Allele Identifier: CA2694839904

Gene: F9

Linked Data

• gnomAD v4: X-139562118-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562121del , CM000685.2:g.139562121del	GRCh38
NC_000023.10:g.138644280del , CM000685.1:g.138644280del	GRCh37
NC_000023.9:g.138471946del	NCBI36
NG_007994.1:g.36386del , LRG_556:g.36386del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.*50del MANE Select	ENSP00000218099.2:n.*50del
ENST00000643157.1:n.1723+380del
ENST00000218099.6:c.*50del	ENSP00000218099.2:n.*50del
NM_000133.3:c.*50del , LRG_556t1:c.*50del	NP_000124.1:n.*50del
NM_001313913.1:c.*50del	NP_001300842.1:n.*50del
XM_005262397.3:c.*50del	XP_005262454.1:n.*50del
XM_005262397.4:c.*50del	XP_005262454.1:n.*50del
NM_000133.4:c.*50del MANE Select	NP_000124.1:n.*50del
NM_001313913.2:c.*50del	NP_001300842.1:n.*50del