Canonical Allele Identifier: CA10529893

Gene: F9

Linked Data

• dbSNP Id: rs773763151
• ExAC: X:138644228 T / TAATG
• gnomAD v2: X-138644228-T-TAATG
• MyVariant Identifiers: chrX:g.138644228_138644229insAATG (hg19) ; chrX:g.139562069_139562070insAATG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562072_139562075dup , CM000685.2:g.139562072_139562075dup	GRCh38
NC_000023.10:g.138644231_138644234dup , CM000685.1:g.138644231_138644234dup	GRCh37
NC_000023.9:g.138471897_138471900dup	NCBI36
NG_007994.1:g.36337_36340dup , LRG_556:g.36337_36340dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.*1_*4dup MANE Select	ENSP00000218099.2:n.*1_*4dup
ENST00000643157.1:n.1723+331_1723+334dup
ENST00000218099.6:c.*1_*4dup	ENSP00000218099.2:n.*1_*4dup
NM_000133.3:c.*1_*4dup , LRG_556t1:c.*1_*4dup	NP_000124.1:n.*1_*4dup
NM_001313913.1:c.*1_*4dup	NP_001300842.1:n.*1_*4dup
XM_005262397.3:c.*1_*4dup	XP_005262454.1:n.*1_*4dup
XM_005262397.4:c.*1_*4dup	XP_005262454.1:n.*1_*4dup
NM_000133.4:c.*1_*4dup MANE Select	NP_000124.1:n.*1_*4dup
NM_001313913.2:c.*1_*4dup	NP_001300842.1:n.*1_*4dup