Canonical Allele Identifier: CA3008768235

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561589_139561590insCCCTGAAAGTTCTGTTTATATTGTGGTG , CM000685.2:g.139561589_139561590insCCCTGAAAGTTCTGTTTATATTGTGGTG	GRCh38
NC_000023.10:g.138643748_138643749insCCCTGAAAGTTCTGTTTATATTGTGGTG , CM000685.1:g.138643748_138643749insCCCTGAAAGTTCTGTTTATATTGTGGTG	GRCh37
NC_000023.9:g.138471414_138471415insCCCTGAAAGTTCTGTTTATATTGTGGTG	NCBI36
NG_007994.1:g.35854_35855insCCCTGAAAGTTCTGTTTATATTGTGGTG , LRG_556:g.35854_35855insCCCTGAAAGTTCTGTTTATATTGTGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.904_905insCCCTGAAAGTTCTGTTTATATTGTGGTG MANE Select	ENSP00000218099.2:p.His302ProfsTer10
ENST00000643157.1:n.1571_1572insCCCTGAAAGTTCTGTTTATATTGTGGTG
ENST00000218099.6:c.904_905insCCCTGAAAGTTCTGTTTATATTGTGGTG	ENSP00000218099.2:p.His302ProfsTer10
ENST00000394090.2:c.790_791insCCCTGAAAGTTCTGTTTATATTGTGGTG	ENSP00000377650.2:p.His264ProfsTer10
NM_000133.3:c.904_905insCCCTGAAAGTTCTGTTTATATTGTGGTG , LRG_556t1:c.904_905insCCCTGAAAGTTCTGTTTATATTGTGGTG	NP_000124.1:p.His302ProfsTer10
NM_001313913.1:c.790_791insCCCTGAAAGTTCTGTTTATATTGTGGTG	NP_001300842.1:p.His264ProfsTer10
XM_005262397.3:c.775_776insCCCTGAAAGTTCTGTTTATATTGTGGTG	XP_005262454.1:p.His259ProfsTer10
XM_005262397.4:c.775_776insCCCTGAAAGTTCTGTTTATATTGTGGTG	XP_005262454.1:p.His259ProfsTer10
NM_000133.4:c.904_905insCCCTGAAAGTTCTGTTTATATTGTGGTG MANE Select	NP_000124.1:p.His302ProfsTer10
NM_001313913.2:c.790_791insCCCTGAAAGTTCTGTTTATATTGTGGTG	NP_001300842.1:p.His264ProfsTer10