Canonical Allele Identifier: CA2461407758

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548339_139548340delinsTA , CM000685.2:g.139548339_139548340delinsTA	GRCh38
NC_000023.10:g.138630498_138630499delinsTA , CM000685.1:g.138630498_138630499delinsTA	GRCh37
NC_000023.9:g.138458164_138458165delinsTA	NCBI36
NG_007994.1:g.22604_22605delinsTA , LRG_556:g.22604_22605delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-24_392-23delinsTA MANE Select	ENSP00000218099.2:n.392-24_392-23delinsTA
ENST00000643157.1:n.1059-24_1059-23delinsTA
ENST00000218099.6:c.392-24_392-23delinsTA	ENSP00000218099.2:n.392-24_392-23delinsTA
ENST00000394090.2:c.278-24_278-23delinsTA	ENSP00000377650.2:n.278-24_278-23delinsTA
ENST00000479617.2:n.345-24_345-23delinsTA
NM_000133.3:c.392-24_392-23delinsTA , LRG_556t1:c.392-24_392-23delinsTA	NP_000124.1:n.392-24_392-23delinsTA
NM_001313913.1:c.278-24_278-23delinsTA	NP_001300842.1:n.278-24_278-23delinsTA
XM_005262397.3:c.392-2723_392-2722delinsTA	XP_005262454.1:n.392-2723_392-2722delinsTA
XM_005262397.4:c.392-2723_392-2722delinsTA	XP_005262454.1:n.392-2723_392-2722delinsTA
NM_000133.4:c.392-24_392-23delinsTA MANE Select	NP_000124.1:n.392-24_392-23delinsTA
NM_001313913.2:c.278-24_278-23delinsTA	NP_001300842.1:n.278-24_278-23delinsTA