Canonical Allele Identifier: CA2823819910

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548328_139548329dup , CM000685.2:g.139548328_139548329dup	GRCh38
NC_000023.10:g.138630487_138630488dup , CM000685.1:g.138630487_138630488dup	GRCh37
NC_000023.9:g.138458153_138458154dup	NCBI36
NG_007994.1:g.22593_22594dup , LRG_556:g.22593_22594dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-35_392-34dup MANE Select	ENSP00000218099.2:n.392-35_392-34dup
ENST00000643157.1:n.1059-35_1059-34dup
ENST00000218099.6:c.392-35_392-34dup	ENSP00000218099.2:n.392-35_392-34dup
ENST00000394090.2:c.278-35_278-34dup	ENSP00000377650.2:n.278-35_278-34dup
ENST00000479617.2:n.345-35_345-34dup
NM_000133.3:c.392-35_392-34dup , LRG_556t1:c.392-35_392-34dup	NP_000124.1:n.392-35_392-34dup
NM_001313913.1:c.278-35_278-34dup	NP_001300842.1:n.278-35_278-34dup
XM_005262397.3:c.392-2734_392-2733dup	XP_005262454.1:n.392-2734_392-2733dup
XM_005262397.4:c.392-2734_392-2733dup	XP_005262454.1:n.392-2734_392-2733dup
NM_000133.4:c.392-35_392-34dup MANE Select	NP_000124.1:n.392-35_392-34dup
NM_001313913.2:c.278-35_278-34dup	NP_001300842.1:n.278-35_278-34dup