Canonical Allele Identifier: CA2695236304

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561652_139561659del , CM000685.2:g.139561652_139561659del	GRCh38
NC_000023.10:g.138643811_138643818del , CM000685.1:g.138643811_138643818del	GRCh37
NC_000023.9:g.138471477_138471484del	NCBI36
NG_007994.1:g.35917_35924del , LRG_556:g.35917_35924del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.967_974del MANE Select	ENSP00000218099.2:p.Glu323SerfsTer13
ENST00000643157.1:n.1634_1641del
ENST00000218099.6:c.967_974del	ENSP00000218099.2:p.Glu323SerfsTer13
ENST00000394090.2:c.853_860del	ENSP00000377650.2:p.Glu285SerfsTer13
NM_000133.3:c.967_974del , LRG_556t1:c.967_974del	NP_000124.1:p.Glu323SerfsTer13
NM_001313913.1:c.853_860del	NP_001300842.1:p.Glu285SerfsTer13
XM_005262397.3:c.838_845del	XP_005262454.1:p.Glu280SerfsTer13
XM_005262397.4:c.838_845del	XP_005262454.1:p.Glu280SerfsTer13
NM_000133.4:c.967_974del MANE Select	NP_000124.1:p.Glu323SerfsTer13
NM_001313913.2:c.853_860del	NP_001300842.1:p.Glu285SerfsTer13