Canonical Allele Identifier: CA645613295

Gene: F9

Linked Data

• dbSNP Id: rs1312779174
• COSMIC: COSM4682264
• MyVariant Identifiers: chrX:g.138644211del (hg19) ; chrX:g.139562052del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562057del , CM000685.2:g.139562057del	GRCh38
NC_000023.10:g.138644216del , CM000685.1:g.138644216del	GRCh37
NC_000023.9:g.138471882del	NCBI36
NG_007994.1:g.36322del , LRG_556:g.36322del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1372del MANE Select	ENSP00000218099.2:p.Thr458GlnfsTer25
ENST00000643157.1:n.1723+316del
ENST00000218099.6:c.1372del	ENSP00000218099.2:p.Thr458GlnfsTer25
ENST00000394090.2:c.1258del	ENSP00000377650.2:p.Thr420GlnfsTer?
NM_000133.3:c.1372del , LRG_556t1:c.1372del	NP_000124.1:p.Thr458GlnfsTer25
NM_001313913.1:c.1258del	NP_001300842.1:p.Thr420GlnfsTer25
XM_005262397.3:c.1243del	XP_005262454.1:p.Thr415GlnfsTer25
XM_005262397.4:c.1243del	XP_005262454.1:p.Thr415GlnfsTer25
NM_000133.4:c.1372del MANE Select	NP_000124.1:p.Thr458GlnfsTer25
NM_001313913.2:c.1258del	NP_001300842.1:p.Thr420GlnfsTer25