Canonical Allele Identifier: CA645125646

Gene: F9

Linked Data

• gnomAD v2: X-138619327-A-AACATCAT
• MyVariant Identifiers: chrX:g.138619327_138619328insACATCAT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537168_139537169insACATCAT , CM000685.2:g.139537168_139537169insACATCAT	GRCh38
NC_000023.10:g.138619327_138619328insACATCAT , CM000685.1:g.138619327_138619328insACATCAT	GRCh37
NC_000023.9:g.138446993_138446994insACATCAT	NCBI36
NG_007994.1:g.11433_11434insACATCAT , LRG_556:g.11433_11434insACATCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.247_248insACATCAT MANE Select	ENSP00000218099.2:p.Arg83AsnfsTer6
ENST00000218099.6:c.247_248insACATCAT	ENSP00000218099.2:p.Arg83AsnfsTer6
ENST00000394090.2:c.247_248insACATCAT	ENSP00000377650.2:p.Arg83AsnfsTer6
ENST00000479617.2:n.241+13_241+14insACATCAT
NM_000133.3:c.247_248insACATCAT , LRG_556t1:c.247_248insACATCAT	NP_000124.1:p.Arg83AsnfsTer6
NM_001313913.1:c.247_248insACATCAT	NP_001300842.1:p.Arg83AsnfsTer6
XM_005262397.3:c.247_248insACATCAT	XP_005262454.1:p.Arg83AsnfsTer6
XM_005262397.4:c.247_248insACATCAT	XP_005262454.1:p.Arg83AsnfsTer6
NM_000133.4:c.247_248insACATCAT MANE Select	NP_000124.1:p.Arg83AsnfsTer6
NM_001313913.2:c.247_248insACATCAT	NP_001300842.1:p.Arg83AsnfsTer6