Canonical Allele Identifier: CA2461412309

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562051_139562052delinsGA , CM000685.2:g.139562051_139562052delinsGA	GRCh38
NC_000023.10:g.138644210_138644211delinsGA , CM000685.1:g.138644210_138644211delinsGA	GRCh37
NC_000023.9:g.138471876_138471877delinsGA	NCBI36
NG_007994.1:g.36316_36317delinsGA , LRG_556:g.36316_36317delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1366_1367delinsGA MANE Select	ENSP00000218099.2:p.Glu456=
ENST00000643157.1:n.1723+310_1723+311delinsGA
ENST00000218099.6:c.1366_1367delinsGA	ENSP00000218099.2:p.Glu456=
ENST00000394090.2:c.1252_1253delinsGA	ENSP00000377650.2:p.Glu418=
NM_000133.3:c.1366_1367delinsGA , LRG_556t1:c.1366_1367delinsGA	NP_000124.1:p.Glu456=
NM_001313913.1:c.1252_1253delinsGA	NP_001300842.1:p.Glu418=
XM_005262397.3:c.1237_1238delinsGA	XP_005262454.1:p.Glu413=
XM_005262397.4:c.1237_1238delinsGA	XP_005262454.1:p.Glu413=
NM_000133.4:c.1366_1367delinsGA MANE Select	NP_000124.1:p.Glu456=
NM_001313913.2:c.1252_1253delinsGA	NP_001300842.1:p.Glu418=