Canonical Allele Identifier: CA645571955
Gene: F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725917_46725918del , CM000673.2:g.46725917_46725918del GRCh38
NC_000011.9:g.46747467_46747468del , CM000673.1:g.46747467_46747468del GRCh37
NC_000011.8:g.46704043_46704044del NCBI36
NG_008953.1:g.11725_11726del , LRG_551:g.11725_11726del

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.618_619del MANE Select ENSP00000308541.5:p.Ser207ThrfsTer9
ENST00000311907.9:c.618_619del ENSP00000308541.5:p.Ser207ThrfsTer9
ENST00000442468.1:c.588_589del ENSP00000387413.1:p.Ser197ThrfsTer9
ENST00000490274.1:n.398_399del
ENST00000530231.5:c.618_619del ENSP00000433907.1:p.Ser207ThrfsTer9
NM_000506.3:c.618_619del NP_000497.1:p.Ser207ThrfsTer9
NM_000506.4:c.618_619del , LRG_551t1:c.618_619del NP_000497.1:p.Ser207ThrfsTer9
NM_001311257.1:c.570_571del NP_001298186.1:p.Ser191ThrfsTer9
XR_428840.2:n.662_663del
XR_428840.4:n.653_654del
NM_000506.5:c.618_619del MANE Select NP_000497.1:p.Ser207ThrfsTer9
NM_001311257.2:c.570_571del NP_001298186.1:p.Ser191ThrfsTer9