Canonical Allele Identifier: CA872127561

Gene: F9

Linked Data

• dbSNP Id: rs1357995025
• MyVariant Identifiers: chrX:g.138643712_138643713del (hg19) ; chrX:g.139561553_139561554del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561554_139561555del , CM000685.2:g.139561554_139561555del	GRCh38
NC_000023.10:g.138643713_138643714del , CM000685.1:g.138643713_138643714del	GRCh37
NC_000023.9:g.138471379_138471380del	NCBI36
NG_007994.1:g.35819_35820del , LRG_556:g.35819_35820del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.869_870del MANE Select	ENSP00000218099.2:p.Thr290ArgfsTer20
ENST00000643157.1:n.1536_1537del
ENST00000218099.6:c.869_870del	ENSP00000218099.2:p.Thr290ArgfsTer20
ENST00000394090.2:c.755_756del	ENSP00000377650.2:p.Thr252ArgfsTer20
NM_000133.3:c.869_870del , LRG_556t1:c.869_870del	NP_000124.1:p.Thr290ArgfsTer20
NM_001313913.1:c.755_756del	NP_001300842.1:p.Thr252ArgfsTer20
XM_005262397.3:c.740_741del	XP_005262454.1:p.Thr247ArgfsTer20
XM_005262397.4:c.740_741del	XP_005262454.1:p.Thr247ArgfsTer20
NM_000133.4:c.869_870del MANE Select	NP_000124.1:p.Thr290ArgfsTer20
NM_001313913.2:c.755_756del	NP_001300842.1:p.Thr252ArgfsTer20