Canonical Allele Identifier: CA2695236315

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541151_139541156dup , CM000685.2:g.139541151_139541156dup	GRCh38
NC_000023.10:g.138623310_138623315dup , CM000685.1:g.138623310_138623315dup	GRCh37
NC_000023.9:g.138450976_138450981dup	NCBI36
NG_007994.1:g.15416_15421dup , LRG_556:g.15416_15421dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.353_358dup MANE Select	ENSP00000218099.2:p.Cys119_Pro120insArgCys
ENST00000218099.6:c.353_358dup	ENSP00000218099.2:p.Cys119_Pro120insArgCys
ENST00000394090.2:c.277+3765_277+3770dup	ENSP00000377650.2:n.277+3765_277+3770dup
ENST00000479617.2:n.306_311dup
NM_000133.3:c.353_358dup , LRG_556t1:c.353_358dup	NP_000124.1:p.Cys119_Pro120insArgCys
NM_001313913.1:c.277+3765_277+3770dup	NP_001300842.1:n.277+3765_277+3770dup
XM_005262397.3:c.353_358dup	XP_005262454.1:p.Cys119_Pro120insArgCys
XM_005262397.4:c.353_358dup	XP_005262454.1:p.Cys119_Pro120insArgCys
NM_000133.4:c.353_358dup MANE Select	NP_000124.1:p.Cys119_Pro120insArgCys
NM_001313913.2:c.277+3765_277+3770dup	NP_001300842.1:n.277+3765_277+3770dup