Canonical Allele Identifier: CA2461407759

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548340_139548344delinsACTGT , CM000685.2:g.139548340_139548344delinsACTGT	GRCh38
NC_000023.10:g.138630499_138630503delinsACTGT , CM000685.1:g.138630499_138630503delinsACTGT	GRCh37
NC_000023.9:g.138458165_138458169delinsACTGT	NCBI36
NG_007994.1:g.22605_22609delinsACTGT , LRG_556:g.22605_22609delinsACTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-23_392-19delinsACTGT MANE Select	ENSP00000218099.2:n.392-23_392-19delinsACTGT
ENST00000643157.1:n.1059-23_1059-19delinsACTGT
ENST00000218099.6:c.392-23_392-19delinsACTGT	ENSP00000218099.2:n.392-23_392-19delinsACTGT
ENST00000394090.2:c.278-23_278-19delinsACTGT	ENSP00000377650.2:n.278-23_278-19delinsACTGT
ENST00000479617.2:n.345-23_345-19delinsACTGT
NM_000133.3:c.392-23_392-19delinsACTGT , LRG_556t1:c.392-23_392-19delinsACTGT	NP_000124.1:n.392-23_392-19delinsACTGT
NM_001313913.1:c.278-23_278-19delinsACTGT	NP_001300842.1:n.278-23_278-19delinsACTGT
XM_005262397.3:c.392-2722_392-2718delinsACTGT	XP_005262454.1:n.392-2722_392-2718delinsACTGT
XM_005262397.4:c.392-2722_392-2718delinsACTGT	XP_005262454.1:n.392-2722_392-2718delinsACTGT
NM_000133.4:c.392-23_392-19delinsACTGT MANE Select	NP_000124.1:n.392-23_392-19delinsACTGT
NM_001313913.2:c.278-23_278-19delinsACTGT	NP_001300842.1:n.278-23_278-19delinsACTGT