Canonical Allele Identifier: CA1969072671

Gene: F2

Linked Data

• dbSNP Id: rs2064874254

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726515_46726517del , CM000673.2:g.46726515_46726517del	GRCh38
NC_000011.9:g.46748065_46748067del , CM000673.1:g.46748065_46748067del	GRCh37
NC_000011.8:g.46704641_46704643del	NCBI36
NG_008953.1:g.12323_12325del , LRG_551:g.12323_12325del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.892_894del MANE Select	ENSP00000308541.5:p.Glu298del
ENST00000311907.9:c.892_894del	ENSP00000308541.5:p.Glu298del
ENST00000442468.1:c.862_864del	ENSP00000387413.1:p.Glu288del
ENST00000530231.5:c.892_894del	ENSP00000433907.1:p.Glu298del
NM_000506.3:c.892_894del	NP_000497.1:p.Glu298del
NM_000506.4:c.892_894del , LRG_551t1:c.892_894del	NP_000497.1:p.Glu298del
NM_001311257.1:c.844_846del	NP_001298186.1:p.Glu282del
XR_428840.2:n.936_938del
XR_428840.4:n.927_929del
NM_000506.5:c.892_894del MANE Select	NP_000497.1:p.Glu298del
NM_001311257.2:c.844_846del	NP_001298186.1:p.Glu282del