Canonical Allele Identifier: CA2695236228

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560752del , CM000685.2:g.139560752del	GRCh38
NC_000023.10:g.138642911del , CM000685.1:g.138642911del	GRCh37
NC_000023.9:g.138470577del	NCBI36
NG_007994.1:g.35017del , LRG_556:g.35017del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.735del MANE Select	ENSP00000218099.2:p.Asn245LysfsTer19
ENST00000643157.1:n.1402del
ENST00000218099.6:c.735del	ENSP00000218099.2:p.Asn245LysfsTer19
ENST00000394090.2:c.621del	ENSP00000377650.2:p.Asn207LysfsTer19
NM_000133.3:c.735del , LRG_556t1:c.735del	NP_000124.1:p.Asn245LysfsTer19
NM_001313913.1:c.621del	NP_001300842.1:p.Asn207LysfsTer19
XM_005262397.3:c.606del	XP_005262454.1:p.Asn202LysfsTer19
XM_005262397.4:c.606del	XP_005262454.1:p.Asn202LysfsTer19
NM_000133.4:c.735del MANE Select	NP_000124.1:p.Asn245LysfsTer19
NM_001313913.2:c.621del	NP_001300842.1:p.Asn207LysfsTer19