Canonical Allele Identifier: CA2574810777

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725768_46725771del , CM000673.2:g.46725768_46725771del	GRCh38
NC_000011.9:g.46747318_46747321del , CM000673.1:g.46747318_46747321del	GRCh37
NC_000011.8:g.46703894_46703897del	NCBI36
NG_008953.1:g.11576_11579del , LRG_551:g.11576_11579del

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.560-91_560-88del MANE Select	ENSP00000308541.5:n.560-91_560-88del
ENST00000311907.9:c.560-91_560-88del	ENSP00000308541.5:n.560-91_560-88del
ENST00000442468.1:c.530-91_530-88del	ENSP00000387413.1:n.530-91_530-88del
ENST00000490274.1:n.340-91_340-88del
ENST00000530231.5:c.560-91_560-88del	ENSP00000433907.1:n.560-91_560-88del
NM_000506.3:c.560-91_560-88del	NP_000497.1:n.560-91_560-88del
NM_000506.4:c.560-91_560-88del , LRG_551t1:c.560-91_560-88del	NP_000497.1:n.560-91_560-88del
NM_001311257.1:c.512-91_512-88del	NP_001298186.1:n.512-91_512-88del
XR_428840.2:n.604-91_604-88del
XR_428840.4:n.595-91_595-88del
NM_000506.5:c.560-91_560-88del MANE Select	NP_000497.1:n.560-91_560-88del
NM_001311257.2:c.512-91_512-88del	NP_001298186.1:n.512-91_512-88del