Canonical Allele Identifier: CA2695236395

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561927_139561929delinsAAT , CM000685.2:g.139561927_139561929delinsAAT	GRCh38
NC_000023.10:g.138644086_138644088delinsAAT , CM000685.1:g.138644086_138644088delinsAAT	GRCh37
NC_000023.9:g.138471752_138471754delinsAAT	NCBI36
NG_007994.1:g.36192_36194delinsAAT , LRG_556:g.36192_36194delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1242_1244delinsAAT MANE Select	ENSP00000218099.2:p.His415Ile
ENST00000643157.1:n.1723+186_1723+188delinsAAT
ENST00000218099.6:c.1242_1244delinsAAT	ENSP00000218099.2:p.His415Ile
ENST00000394090.2:c.1128_1130delinsAAT	ENSP00000377650.2:p.His377Ile
NM_000133.3:c.1242_1244delinsAAT , LRG_556t1:c.1242_1244delinsAAT	NP_000124.1:p.His415Ile
NM_001313913.1:c.1128_1130delinsAAT	NP_001300842.1:p.His377Ile
XM_005262397.3:c.1113_1115delinsAAT	XP_005262454.1:p.His372Ile
XM_005262397.4:c.1113_1115delinsAAT	XP_005262454.1:p.His372Ile
NM_000133.4:c.1242_1244delinsAAT MANE Select	NP_000124.1:p.His415Ile
NM_001313913.2:c.1128_1130delinsAAT	NP_001300842.1:p.His377Ile