Canonical Allele Identifier: CA915952339

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139530802del , CM000685.2:g.139530802del	GRCh38
NC_000023.10:g.138612961del , CM000685.1:g.138612961del	GRCh37
NC_000023.9:g.138440627del	NCBI36
NG_007994.1:g.5067del , LRG_556:g.5067del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.38del MANE Select	ENSP00000218099.2:p.Gly13AlafsTer8
ENST00000218099.6:c.38del	ENSP00000218099.2:p.Gly13AlafsTer8
ENST00000394090.2:c.38del	ENSP00000377650.2:p.Gly13AlafsTer8
ENST00000479617.2:n.45del
NM_000133.3:c.38del , LRG_556t1:c.38del	NP_000124.1:p.Gly13AlafsTer8
NM_001313913.1:c.38del	NP_001300842.1:p.Gly13AlafsTer8
XM_005262397.3:c.38del	XP_005262454.1:p.Gly13AlafsTer8
XM_005262397.4:c.38del	XP_005262454.1:p.Gly13AlafsTer8
NM_000133.4:c.38del MANE Select	NP_000124.1:p.Gly13AlafsTer8
NM_001313913.2:c.38del	NP_001300842.1:p.Gly13AlafsTer8