Canonical Allele Identifier: CA2695236214

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537151_139537152delinsA , CM000685.2:g.139537151_139537152delinsA	GRCh38
NC_000023.10:g.138619310_138619311delinsA , CM000685.1:g.138619310_138619311delinsA	GRCh37
NC_000023.9:g.138446976_138446977delinsA	NCBI36
NG_007994.1:g.11416_11417delinsA , LRG_556:g.11416_11417delinsA

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.230_231delinsA MANE Select	ENSP00000218099.2:p.Val77AspfsTer27
ENST00000218099.6:c.230_231delinsA	ENSP00000218099.2:p.Val77AspfsTer27
ENST00000394090.2:c.230_231delinsA	ENSP00000377650.2:p.Val77AspfsTer18
ENST00000479617.2:n.237_238delinsA
NM_000133.3:c.230_231delinsA , LRG_556t1:c.230_231delinsA	NP_000124.1:p.Val77AspfsTer27
NM_001313913.1:c.230_231delinsA	NP_001300842.1:p.Val77AspfsTer18
XM_005262397.3:c.230_231delinsA	XP_005262454.1:p.Val77AspfsTer27
XM_005262397.4:c.230_231delinsA	XP_005262454.1:p.Val77AspfsTer27
NM_000133.4:c.230_231delinsA MANE Select	NP_000124.1:p.Val77AspfsTer27
NM_001313913.2:c.230_231delinsA	NP_001300842.1:p.Val77AspfsTer18