Canonical Allele Identifier: CA2579713724

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548481_139548482del , CM000685.2:g.139548481_139548482del	GRCh38
NC_000023.10:g.138630640_138630641del , CM000685.1:g.138630640_138630641del	GRCh37
NC_000023.9:g.138458306_138458307del	NCBI36
NG_007994.1:g.22746_22747del , LRG_556:g.22746_22747del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.510_511del MANE Select	ENSP00000218099.2:p.Cys170Ter
ENST00000643157.1:n.1177_1178del
ENST00000218099.6:c.510_511del	ENSP00000218099.2:p.Cys170Ter
ENST00000394090.2:c.396_397del	ENSP00000377650.2:p.Cys132Ter
NM_000133.3:c.510_511del , LRG_556t1:c.510_511del	NP_000124.1:p.Cys170Ter
NM_001313913.1:c.396_397del	NP_001300842.1:p.Cys132Ter
XM_005262397.3:c.392-2581_392-2580del	XP_005262454.1:n.392-2581_392-2580del
XM_005262397.4:c.392-2581_392-2580del	XP_005262454.1:n.392-2581_392-2580del
NM_000133.4:c.510_511del MANE Select	NP_000124.1:p.Cys170Ter
NM_001313913.2:c.396_397del	NP_001300842.1:p.Cys132Ter