Canonical Allele Identifier: CA2694839939

Gene: F9

Linked Data

• gnomAD v4: X-139562202-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562206del , CM000685.2:g.139562206del	GRCh38
NC_000023.10:g.138644365del , CM000685.1:g.138644365del	GRCh37
NC_000023.9:g.138472031del	NCBI36
NG_007994.1:g.36471del , LRG_556:g.36471del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.*135del MANE Select	ENSP00000218099.2:n.*135del
ENST00000643157.1:n.1723+465del
ENST00000218099.6:c.*135del	ENSP00000218099.2:n.*135del
NM_000133.3:c.*135del , LRG_556t1:c.*135del	NP_000124.1:n.*135del
NM_001313913.1:c.*135del	NP_001300842.1:n.*135del
XM_005262397.3:c.*135del	XP_005262454.1:n.*135del
XM_005262397.4:c.*135del	XP_005262454.1:n.*135del
NM_000133.4:c.*135del MANE Select	NP_000124.1:n.*135del
NM_001313913.2:c.*135del	NP_001300842.1:n.*135del