Canonical Allele Identifier: CA2461408640

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551228_139551231delinsTGGA , CM000685.2:g.139551228_139551231delinsTGGA	GRCh38
NC_000023.10:g.138633387_138633390delinsTGGA , CM000685.1:g.138633387_138633390delinsTGGA	GRCh37
NC_000023.9:g.138461053_138461056delinsTGGA	NCBI36
NG_007994.1:g.25493_25496delinsTGGA , LRG_556:g.25493_25496delinsTGGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.687_690delinsTGGA MANE Select	ENSP00000218099.2:p.Gly229=
ENST00000643157.1:n.1354_1357delinsTGGA
ENST00000218099.6:c.687_690delinsTGGA	ENSP00000218099.2:p.Gly229=
ENST00000394090.2:c.573_576delinsTGGA	ENSP00000377650.2:p.Gly191=
NM_000133.3:c.687_690delinsTGGA , LRG_556t1:c.687_690delinsTGGA	NP_000124.1:p.Gly229=
NM_001313913.1:c.573_576delinsTGGA	NP_001300842.1:p.Gly191=
XM_005262397.3:c.558_561delinsTGGA	XP_005262454.1:p.Gly186=
XM_005262397.4:c.558_561delinsTGGA	XP_005262454.1:p.Gly186=
NM_000133.4:c.687_690delinsTGGA MANE Select	NP_000124.1:p.Gly229=
NM_001313913.2:c.573_576delinsTGGA	NP_001300842.1:p.Gly191=