Canonical Allele Identifier: CA2461408550

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139550932_139550933delinsAT , CM000685.2:g.139550932_139550933delinsAT	GRCh38
NC_000023.10:g.138633091_138633092delinsAT , CM000685.1:g.138633091_138633092delinsAT	GRCh37
NC_000023.9:g.138460757_138460758delinsAT	NCBI36
NG_007994.1:g.25197_25198delinsAT , LRG_556:g.25197_25198delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.521-130_521-129delinsAT MANE Select	ENSP00000218099.2:n.521-130_521-129delinsAT
ENST00000643157.1:n.1188-130_1188-129delinsAT
ENST00000218099.6:c.521-130_521-129delinsAT	ENSP00000218099.2:n.521-130_521-129delinsAT
ENST00000394090.2:c.407-130_407-129delinsAT	ENSP00000377650.2:n.407-130_407-129delinsAT
NM_000133.3:c.521-130_521-129delinsAT , LRG_556t1:c.521-130_521-129delinsAT	NP_000124.1:n.521-130_521-129delinsAT
NM_001313913.1:c.407-130_407-129delinsAT	NP_001300842.1:n.407-130_407-129delinsAT
XM_005262397.3:c.392-130_392-129delinsAT	XP_005262454.1:n.392-130_392-129delinsAT
XM_005262397.4:c.392-130_392-129delinsAT	XP_005262454.1:n.392-130_392-129delinsAT
NM_000133.4:c.521-130_521-129delinsAT MANE Select	NP_000124.1:n.521-130_521-129delinsAT
NM_001313913.2:c.407-130_407-129delinsAT	NP_001300842.1:n.407-130_407-129delinsAT