Canonical Allele Identifier: CA2461412153

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561740_139561742delinsATG , CM000685.2:g.139561740_139561742delinsATG	GRCh38
NC_000023.10:g.138643899_138643901delinsATG , CM000685.1:g.138643899_138643901delinsATG	GRCh37
NC_000023.9:g.138471565_138471567delinsATG	NCBI36
NG_007994.1:g.36005_36007delinsATG , LRG_556:g.36005_36007delinsATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1055_1057delinsATG MANE Select	ENSP00000218099.2:p.Tyr352=
ENST00000643157.1:n.1722_1723+1delinsATG
ENST00000218099.6:c.1055_1057delinsATG	ENSP00000218099.2:p.Tyr352=
ENST00000394090.2:c.941_943delinsATG	ENSP00000377650.2:p.Tyr314=
NM_000133.3:c.1055_1057delinsATG , LRG_556t1:c.1055_1057delinsATG	NP_000124.1:p.Tyr352=
NM_001313913.1:c.941_943delinsATG	NP_001300842.1:p.Tyr314=
XM_005262397.3:c.926_928delinsATG	XP_005262454.1:p.Tyr309=
XM_005262397.4:c.926_928delinsATG	XP_005262454.1:p.Tyr309=
NM_000133.4:c.1055_1057delinsATG MANE Select	NP_000124.1:p.Tyr352=
NM_001313913.2:c.941_943delinsATG	NP_001300842.1:p.Tyr314=