Canonical Allele Identifier: CA3039260800

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561482_139561485del , CM000685.2:g.139561482_139561485del	GRCh38
NC_000023.10:g.138643641_138643644del , CM000685.1:g.138643641_138643644del	GRCh37
NC_000023.9:g.138471307_138471310del	NCBI36
NG_007994.1:g.35747_35750del , LRG_556:g.35747_35750del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.839-42_839-39del MANE Select	ENSP00000218099.2:n.839-42_839-39del
ENST00000643157.1:n.1506-42_1506-39del
ENST00000218099.6:c.839-42_839-39del	ENSP00000218099.2:n.839-42_839-39del
ENST00000394090.2:c.725-42_725-39del	ENSP00000377650.2:n.725-42_725-39del
NM_000133.3:c.839-42_839-39del , LRG_556t1:c.839-42_839-39del	NP_000124.1:n.839-42_839-39del
NM_001313913.1:c.725-42_725-39del	NP_001300842.1:n.725-42_725-39del
XM_005262397.3:c.710-42_710-39del	XP_005262454.1:n.710-42_710-39del
XM_005262397.4:c.710-42_710-39del	XP_005262454.1:n.710-42_710-39del
NM_000133.4:c.839-42_839-39del MANE Select	NP_000124.1:n.839-42_839-39del
NM_001313913.2:c.725-42_725-39del	NP_001300842.1:n.725-42_725-39del