Canonical Allele Identifier: CA2695236310

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561675del , CM000685.2:g.139561675del	GRCh38
NC_000023.10:g.138643834del , CM000685.1:g.138643834del	GRCh37
NC_000023.9:g.138471500del	NCBI36
NG_007994.1:g.35940del , LRG_556:g.35940del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.990del MANE Select	ENSP00000218099.2:p.Tyr330Ter
ENST00000643157.1:n.1657del
ENST00000218099.6:c.990del	ENSP00000218099.2:p.Tyr330Ter
ENST00000394090.2:c.876del	ENSP00000377650.2:p.Tyr292Ter
NM_000133.3:c.990del , LRG_556t1:c.990del	NP_000124.1:p.Tyr330Ter
NM_001313913.1:c.876del	NP_001300842.1:p.Tyr292Ter
XM_005262397.3:c.861del	XP_005262454.1:p.Tyr287Ter
XM_005262397.4:c.861del	XP_005262454.1:p.Tyr287Ter
NM_000133.4:c.990del MANE Select	NP_000124.1:p.Tyr330Ter
NM_001313913.2:c.876del	NP_001300842.1:p.Tyr292Ter