Canonical Allele Identifier: CA2461412260

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561943_139561944delinsGA , CM000685.2:g.139561943_139561944delinsGA	GRCh38
NC_000023.10:g.138644102_138644103delinsGA , CM000685.1:g.138644102_138644103delinsGA	GRCh37
NC_000023.9:g.138471768_138471769delinsGA	NCBI36
NG_007994.1:g.36208_36209delinsGA , LRG_556:g.36208_36209delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1258_1259delinsGA MANE Select	ENSP00000218099.2:p.Glu420=
ENST00000643157.1:n.1723+202_1723+203delinsGA
ENST00000218099.6:c.1258_1259delinsGA	ENSP00000218099.2:p.Glu420=
ENST00000394090.2:c.1144_1145delinsGA	ENSP00000377650.2:p.Glu382=
NM_000133.3:c.1258_1259delinsGA , LRG_556t1:c.1258_1259delinsGA	NP_000124.1:p.Glu420=
NM_001313913.1:c.1144_1145delinsGA	NP_001300842.1:p.Glu382=
XM_005262397.3:c.1129_1130delinsGA	XP_005262454.1:p.Glu377=
XM_005262397.4:c.1129_1130delinsGA	XP_005262454.1:p.Glu377=
NM_000133.4:c.1258_1259delinsGA MANE Select	NP_000124.1:p.Glu420=
NM_001313913.2:c.1144_1145delinsGA	NP_001300842.1:p.Glu382=