Canonical Allele Identifier: CA2560145256

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551135_139551139del , CM000685.2:g.139551135_139551139del	GRCh38
NC_000023.10:g.138633294_138633298del , CM000685.1:g.138633294_138633298del	GRCh37
NC_000023.9:g.138460960_138460964del	NCBI36
NG_007994.1:g.25400_25404del , LRG_556:g.25400_25404del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.594_598del MANE Select	ENSP00000218099.2:p.Asp198GlufsTer7
ENST00000643157.1:n.1261_1265del
ENST00000218099.6:c.594_598del	ENSP00000218099.2:p.Asp198GlufsTer7
ENST00000394090.2:c.480_484del	ENSP00000377650.2:p.Asp160GlufsTer7
NM_000133.3:c.594_598del , LRG_556t1:c.594_598del	NP_000124.1:p.Asp198GlufsTer7
NM_001313913.1:c.480_484del	NP_001300842.1:p.Asp160GlufsTer7
XM_005262397.3:c.465_469del	XP_005262454.1:p.Asp155GlufsTer7
XM_005262397.4:c.465_469del	XP_005262454.1:p.Asp155GlufsTer7
NM_000133.4:c.594_598del MANE Select	NP_000124.1:p.Asp198GlufsTer7
NM_001313913.2:c.480_484del	NP_001300842.1:p.Asp160GlufsTer7