Canonical Allele Identifier: CA2518951471

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561495_139561496del , CM000685.2:g.139561495_139561496del	GRCh38
NC_000023.10:g.138643654_138643655del , CM000685.1:g.138643654_138643655del	GRCh37
NC_000023.9:g.138471320_138471321del	NCBI36
NG_007994.1:g.35760_35761del , LRG_556:g.35760_35761del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.839-29_839-28del MANE Select	ENSP00000218099.2:n.839-29_839-28del
ENST00000643157.1:n.1506-29_1506-28del
ENST00000218099.6:c.839-29_839-28del	ENSP00000218099.2:n.839-29_839-28del
ENST00000394090.2:c.725-29_725-28del	ENSP00000377650.2:n.725-29_725-28del
NM_000133.3:c.839-29_839-28del , LRG_556t1:c.839-29_839-28del	NP_000124.1:n.839-29_839-28del
NM_001313913.1:c.725-29_725-28del	NP_001300842.1:n.725-29_725-28del
XM_005262397.3:c.710-29_710-28del	XP_005262454.1:n.710-29_710-28del
XM_005262397.4:c.710-29_710-28del	XP_005262454.1:n.710-29_710-28del
NM_000133.4:c.839-29_839-28del MANE Select	NP_000124.1:n.839-29_839-28del
NM_001313913.2:c.725-29_725-28del	NP_001300842.1:n.725-29_725-28del