Canonical Allele Identifier: CA2695236400

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548467_139548468insC , CM000685.2:g.139548467_139548468insC	GRCh38
NC_000023.10:g.138630626_138630627insC , CM000685.1:g.138630626_138630627insC	GRCh37
NC_000023.9:g.138458292_138458293insC	NCBI36
NG_007994.1:g.22732_22733insC , LRG_556:g.22732_22733insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.496_497insC MANE Select	ENSP00000218099.2:p.Asn166ThrfsTer6
ENST00000643157.1:n.1163_1164insC
ENST00000218099.6:c.496_497insC	ENSP00000218099.2:p.Asn166ThrfsTer6
ENST00000394090.2:c.382_383insC	ENSP00000377650.2:p.Asn128ThrfsTer6
NM_000133.3:c.496_497insC , LRG_556t1:c.496_497insC	NP_000124.1:p.Asn166ThrfsTer6
NM_001313913.1:c.382_383insC	NP_001300842.1:p.Asn128ThrfsTer6
XM_005262397.3:c.392-2595_392-2594insC	XP_005262454.1:n.392-2595_392-2594insC
XM_005262397.4:c.392-2595_392-2594insC	XP_005262454.1:n.392-2595_392-2594insC
NM_000133.4:c.496_497insC MANE Select	NP_000124.1:p.Asn166ThrfsTer6
NM_001313913.2:c.382_383insC	NP_001300842.1:p.Asn128ThrfsTer6