Canonical Allele Identifier: CA1969071809
Gene: F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725794_46725796delinsCCT , CM000673.2:g.46725794_46725796delinsCCT GRCh38
NC_000011.9:g.46747344_46747346delinsCCT , CM000673.1:g.46747344_46747346delinsCCT GRCh37
NC_000011.8:g.46703920_46703922delinsCCT NCBI36
NG_008953.1:g.11602_11604delinsCCT , LRG_551:g.11602_11604delinsCCT

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.560-65_560-63delinsCCT MANE Select ENSP00000308541.5:n.560-65_560-63delinsCC...
ENST00000311907.9:c.560-65_560-63delinsCCT ENSP00000308541.5:n.560-65_560-63delinsCC...
ENST00000442468.1:c.530-65_530-63delinsCCT ENSP00000387413.1:n.530-65_530-63delinsCC...
ENST00000490274.1:n.340-65_340-63delinsCCT
ENST00000530231.5:c.560-65_560-63delinsCCT ENSP00000433907.1:n.560-65_560-63delinsCC...
NM_000506.3:c.560-65_560-63delinsCCT NP_000497.1:n.560-65_560-63delinsCCT
NM_000506.4:c.560-65_560-63delinsCCT , LRG_551t1:c.560-65_560-63delinsCCT NP_000497.1:n.560-65_560-63delinsCCT
NM_001311257.1:c.512-65_512-63delinsCCT NP_001298186.1:n.512-65_512-63delinsCCT
XR_428840.2:n.604-65_604-63delinsCCT
XR_428840.4:n.595-65_595-63delinsCCT
NM_000506.5:c.560-65_560-63delinsCCT MANE Select NP_000497.1:n.560-65_560-63delinsCCT
NM_001311257.2:c.512-65_512-63delinsCCT NP_001298186.1:n.512-65_512-63delinsCCT