Canonical Allele Identifier: CA3039260808

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561498_139561499insCTA , CM000685.2:g.139561498_139561499insCTA	GRCh38
NC_000023.10:g.138643657_138643658insCTA , CM000685.1:g.138643657_138643658insCTA	GRCh37
NC_000023.9:g.138471323_138471324insCTA	NCBI36
NG_007994.1:g.35763_35764insCTA , LRG_556:g.35763_35764insCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.839-26_839-25insCTA MANE Select	ENSP00000218099.2:n.839-26_839-25insCTA
ENST00000643157.1:n.1506-26_1506-25insCTA
ENST00000218099.6:c.839-26_839-25insCTA	ENSP00000218099.2:n.839-26_839-25insCTA
ENST00000394090.2:c.725-26_725-25insCTA	ENSP00000377650.2:n.725-26_725-25insCTA
NM_000133.3:c.839-26_839-25insCTA , LRG_556t1:c.839-26_839-25insCTA	NP_000124.1:n.839-26_839-25insCTA
NM_001313913.1:c.725-26_725-25insCTA	NP_001300842.1:n.725-26_725-25insCTA
XM_005262397.3:c.710-26_710-25insCTA	XP_005262454.1:n.710-26_710-25insCTA
XM_005262397.4:c.710-26_710-25insCTA	XP_005262454.1:n.710-26_710-25insCTA
NM_000133.4:c.839-26_839-25insCTA MANE Select	NP_000124.1:n.839-26_839-25insCTA
NM_001313913.2:c.725-26_725-25insCTA	NP_001300842.1:n.725-26_725-25insCTA