Canonical Allele Identifier: CA1969071937
Gene: F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725891_46725900delinsCGCTCCGAAG , CM000673.2:g.46725891_46725900delinsCGCTCCGAAG GRCh38
NC_000011.9:g.46747441_46747450delinsCGCTCCGAAG , CM000673.1:g.46747441_46747450delinsCGCTCCGAAG GRCh37
NC_000011.8:g.46704017_46704026delinsCGCTCCGAAG NCBI36
NG_008953.1:g.11699_11708delinsCGCTCCGAAG , LRG_551:g.11699_11708delinsCGCTCCGAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.592_601delinsCGCTCCGAAG MANE Select ENSP00000308541.5:p.Arg198=
ENST00000311907.9:c.592_601delinsCGCTCCGAAG ENSP00000308541.5:p.Arg198=
ENST00000442468.1:c.562_571delinsCGCTCCGAAG ENSP00000387413.1:p.Arg188=
ENST00000490274.1:n.372_381delinsCGCTCCGAAG
ENST00000530231.5:c.592_601delinsCGCTCCGAAG ENSP00000433907.1:p.Arg198=
NM_000506.3:c.592_601delinsCGCTCCGAAG NP_000497.1:p.Arg198=
NM_000506.4:c.592_601delinsCGCTCCGAAG , LRG_551t1:c.592_601delinsCGCTCCGAAG NP_000497.1:p.Arg198=
NM_001311257.1:c.544_553delinsCGCTCCGAAG NP_001298186.1:p.Arg182=
XR_428840.2:n.636_645delinsCGCTCCGAAG
XR_428840.4:n.627_636delinsCGCTCCGAAG
NM_000506.5:c.592_601delinsCGCTCCGAAG MANE Select NP_000497.1:p.Arg198=
NM_001311257.2:c.544_553delinsCGCTCCGAAG NP_001298186.1:p.Arg182=