Canonical Allele Identifier: CA2695236339

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561773_139561781delinsA , CM000685.2:g.139561773_139561781delinsA	GRCh38
NC_000023.10:g.138643932_138643940delinsA , CM000685.1:g.138643932_138643940delinsA	GRCh37
NC_000023.9:g.138471598_138471606delinsA	NCBI36
NG_007994.1:g.36038_36046delinsA , LRG_556:g.36038_36046delinsA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1088_1096delinsA MANE Select	ENSP00000218099.2:p.Gly363AspfsTer8
ENST00000643157.1:n.1723+32_1723+40delinsA
ENST00000218099.6:c.1088_1096delinsA	ENSP00000218099.2:p.Gly363AspfsTer8
ENST00000394090.2:c.974_982delinsA	ENSP00000377650.2:p.Gly325AspfsTer8
NM_000133.3:c.1088_1096delinsA , LRG_556t1:c.1088_1096delinsA	NP_000124.1:p.Gly363AspfsTer8
NM_001313913.1:c.974_982delinsA	NP_001300842.1:p.Gly325AspfsTer8
XM_005262397.3:c.959_967delinsA	XP_005262454.1:p.Gly320AspfsTer8
XM_005262397.4:c.959_967delinsA	XP_005262454.1:p.Gly320AspfsTer8
NM_000133.4:c.1088_1096delinsA MANE Select	NP_000124.1:p.Gly363AspfsTer8
NM_001313913.2:c.974_982delinsA	NP_001300842.1:p.Gly325AspfsTer8