Canonical Allele Identifier: CA3039260803

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561491_139561492insCTCCTCAATA , CM000685.2:g.139561491_139561492insCTCCTCAATA	GRCh38
NC_000023.10:g.138643650_138643651insCTCCTCAATA , CM000685.1:g.138643650_138643651insCTCCTCAATA	GRCh37
NC_000023.9:g.138471316_138471317insCTCCTCAATA	NCBI36
NG_007994.1:g.35756_35757insCTCCTCAATA , LRG_556:g.35756_35757insCTCCTCAATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.839-33_839-32insCTCCTCAATA MANE Select	ENSP00000218099.2:n.839-33_839-32insCTCCTCAATA
ENST00000643157.1:n.1506-33_1506-32insCTCCTCAATA
ENST00000218099.6:c.839-33_839-32insCTCCTCAATA	ENSP00000218099.2:n.839-33_839-32insCTCCTCAATA
ENST00000394090.2:c.725-33_725-32insCTCCTCAATA	ENSP00000377650.2:n.725-33_725-32insCTCCTCAATA
NM_000133.3:c.839-33_839-32insCTCCTCAATA , LRG_556t1:c.839-33_839-32insCTCCTCAATA	NP_000124.1:n.839-33_839-32insCTCCTCAATA
NM_001313913.1:c.725-33_725-32insCTCCTCAATA	NP_001300842.1:n.725-33_725-32insCTCCTCAATA
XM_005262397.3:c.710-33_710-32insCTCCTCAATA	XP_005262454.1:n.710-33_710-32insCTCCTCAATA
XM_005262397.4:c.710-33_710-32insCTCCTCAATA	XP_005262454.1:n.710-33_710-32insCTCCTCAATA
NM_000133.4:c.839-33_839-32insCTCCTCAATA MANE Select	NP_000124.1:n.839-33_839-32insCTCCTCAATA
NM_001313913.2:c.725-33_725-32insCTCCTCAATA	NP_001300842.1:n.725-33_725-32insCTCCTCAATA