Canonical Allele Identifier: CA2506060650

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561900_139561901insC , CM000685.2:g.139561900_139561901insC	GRCh38
NC_000023.10:g.138644059_138644060insC , CM000685.1:g.138644059_138644060insC	GRCh37
NC_000023.9:g.138471725_138471726insC	NCBI36
NG_007994.1:g.36165_36166insC , LRG_556:g.36165_36166insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1215_1216insC MANE Select	ENSP00000218099.2:p.Ser406LeufsTer6
ENST00000643157.1:n.1723+159_1723+160insC
ENST00000218099.6:c.1215_1216insC	ENSP00000218099.2:p.Ser406LeufsTer6
ENST00000394090.2:c.1101_1102insC	ENSP00000377650.2:p.Ser368LeufsTer6
NM_000133.3:c.1215_1216insC , LRG_556t1:c.1215_1216insC	NP_000124.1:p.Ser406LeufsTer6
NM_001313913.1:c.1101_1102insC	NP_001300842.1:p.Ser368LeufsTer6
XM_005262397.3:c.1086_1087insC	XP_005262454.1:p.Ser363LeufsTer6
XM_005262397.4:c.1086_1087insC	XP_005262454.1:p.Ser363LeufsTer6
NM_000133.4:c.1215_1216insC MANE Select	NP_000124.1:p.Ser406LeufsTer6
NM_001313913.2:c.1101_1102insC	NP_001300842.1:p.Ser368LeufsTer6