Canonical Allele Identifier: CA2695236201

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551209del , CM000685.2:g.139551209del	GRCh38
NC_000023.10:g.138633368del , CM000685.1:g.138633368del	GRCh37
NC_000023.9:g.138461034del	NCBI36
NG_007994.1:g.25474del , LRG_556:g.25474del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.668del MANE Select	ENSP00000218099.2:p.Asp223AlafsTer22
ENST00000643157.1:n.1335del
ENST00000218099.6:c.668del	ENSP00000218099.2:p.Asp223AlafsTer22
ENST00000394090.2:c.554del	ENSP00000377650.2:p.Asp185AlafsTer22
NM_000133.3:c.668del , LRG_556t1:c.668del	NP_000124.1:p.Asp223AlafsTer22
NM_001313913.1:c.554del	NP_001300842.1:p.Asp185AlafsTer22
XM_005262397.3:c.539del	XP_005262454.1:p.Asp180AlafsTer22
XM_005262397.4:c.539del	XP_005262454.1:p.Asp180AlafsTer22
NM_000133.4:c.668del MANE Select	NP_000124.1:p.Asp223AlafsTer22
NM_001313913.2:c.554del	NP_001300842.1:p.Asp185AlafsTer22