Canonical Allele Identifier: CA5967004
Gene: F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725818dup , CM000673.2:g.46725818dup GRCh38
NC_000011.9:g.46747368dup , CM000673.1:g.46747368dup GRCh37
NC_000011.8:g.46703944dup NCBI36
NG_008953.1:g.11626dup , LRG_551:g.11626dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.560-41dup MANE Select ENSP00000308541.5:n.560-41dup
ENST00000311907.9:c.560-41dup ENSP00000308541.5:n.560-41dup
ENST00000442468.1:c.530-41dup ENSP00000387413.1:n.530-41dup
ENST00000490274.1:n.340-41dup
ENST00000530231.5:c.560-41dup ENSP00000433907.1:n.560-41dup
NM_000506.3:c.560-41dup NP_000497.1:n.560-41dup
NM_000506.4:c.560-41dup , LRG_551t1:c.560-41dup NP_000497.1:n.560-41dup
NM_001311257.1:c.512-41dup NP_001298186.1:n.512-41dup
XR_428840.2:n.604-41dup
XR_428840.4:n.595-41dup
NM_000506.5:c.560-41dup MANE Select NP_000497.1:n.560-41dup
NM_001311257.2:c.512-41dup NP_001298186.1:n.512-41dup