Canonical Allele Identifier: CA2461412251

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561929_139561935delinsATGTTAC , CM000685.2:g.139561929_139561935delinsATGTTAC	GRCh38
NC_000023.10:g.138644088_138644094delinsATGTTAC , CM000685.1:g.138644088_138644094delinsATGTTAC	GRCh37
NC_000023.9:g.138471754_138471760delinsATGTTAC	NCBI36
NG_007994.1:g.36194_36200delinsATGTTAC , LRG_556:g.36194_36200delinsATGTTAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1244_1250delinsATGTTAC MANE Select	ENSP00000218099.2:p.His415=
ENST00000643157.1:n.1723+188_1723+194delinsATGTTAC
ENST00000218099.6:c.1244_1250delinsATGTTAC	ENSP00000218099.2:p.His415=
ENST00000394090.2:c.1130_1136delinsATGTTAC	ENSP00000377650.2:p.His377=
NM_000133.3:c.1244_1250delinsATGTTAC , LRG_556t1:c.1244_1250delinsATGTTAC	NP_000124.1:p.His415=
NM_001313913.1:c.1130_1136delinsATGTTAC	NP_001300842.1:p.His377=
XM_005262397.3:c.1115_1121delinsATGTTAC	XP_005262454.1:p.His372=
XM_005262397.4:c.1115_1121delinsATGTTAC	XP_005262454.1:p.His372=
NM_000133.4:c.1244_1250delinsATGTTAC MANE Select	NP_000124.1:p.His415=
NM_001313913.2:c.1130_1136delinsATGTTAC	NP_001300842.1:p.His377=