Canonical Allele Identifier: CA2823819446

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139540945_139540951del , CM000685.2:g.139540945_139540951del	GRCh38
NC_000023.10:g.138623104_138623110del , CM000685.1:g.138623104_138623110del	GRCh37
NC_000023.9:g.138450770_138450776del	NCBI36
NG_007994.1:g.15210_15216del , LRG_556:g.15210_15216del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.278-131_278-125del MANE Select	ENSP00000218099.2:n.278-131_278-125del
ENST00000218099.6:c.278-131_278-125del	ENSP00000218099.2:n.278-131_278-125del
ENST00000394090.2:c.277+3559_277+3565del	ENSP00000377650.2:n.277+3559_277+3565del
ENST00000479617.2:n.242-142_242-136del
NM_000133.3:c.278-131_278-125del , LRG_556t1:c.278-131_278-125del	NP_000124.1:n.278-131_278-125del
NM_001313913.1:c.277+3559_277+3565del	NP_001300842.1:n.277+3559_277+3565del
XM_005262397.3:c.278-131_278-125del	XP_005262454.1:n.278-131_278-125del
XM_005262397.4:c.278-131_278-125del	XP_005262454.1:n.278-131_278-125del
NM_000133.4:c.278-131_278-125del MANE Select	NP_000124.1:n.278-131_278-125del
NM_001313913.2:c.277+3559_277+3565del	NP_001300842.1:n.277+3559_277+3565del