Canonical Allele Identifier: CA1969072956
Gene: F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46726712_46726714delinsCTG , CM000673.2:g.46726712_46726714delinsCTG GRCh38
NC_000011.9:g.46748262_46748264delinsCTG , CM000673.1:g.46748262_46748264delinsCTG GRCh37
NC_000011.8:g.46704838_46704840delinsCTG NCBI36
NG_008953.1:g.12520_12522delinsCTG , LRG_551:g.12520_12522delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.1005_1007delinsCTG MANE Select ENSP00000308541.5:p.Asp335=
ENST00000311907.9:c.1005_1007delinsCTG ENSP00000308541.5:p.Asp335=
ENST00000530231.5:c.1005_1007delinsCTG ENSP00000433907.1:p.Asp335=
NM_000506.3:c.1005_1007delinsCTG NP_000497.1:p.Asp335=
NM_000506.4:c.1005_1007delinsCTG , LRG_551t1:c.1005_1007delinsCTG NP_000497.1:p.Asp335=
NM_001311257.1:c.957_959delinsCTG NP_001298186.1:p.Asp319=
XR_428840.2:n.1049_1051delinsCTG
XR_428840.4:n.1040_1042delinsCTG
NM_000506.5:c.1005_1007delinsCTG MANE Select NP_000497.1:p.Asp335=
NM_001311257.2:c.957_959delinsCTG NP_001298186.1:p.Asp319=