Canonical Allele Identifier: CA2574810816

Gene: F2

Linked Data

• gnomAD v4: 11-46726523-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726524del , CM000673.2:g.46726524del	GRCh38
NC_000011.9:g.46748074del , CM000673.1:g.46748074del	GRCh37
NC_000011.8:g.46704650del	NCBI36
NG_008953.1:g.12332del , LRG_551:g.12332del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.901del MANE Select	ENSP00000308541.5:p.Asp301MetfsTer?
ENST00000311907.9:c.901del	ENSP00000308541.5:p.Asp301MetfsTer?
ENST00000442468.1:c.871del	ENSP00000387413.1:p.Asp291MetfsTer?
ENST00000530231.5:c.901del	ENSP00000433907.1:p.Asp301MetfsTer?
NM_000506.3:c.901del	NP_000497.1:p.Asp301MetfsTer?
NM_000506.4:c.901del , LRG_551t1:c.901del	NP_000497.1:p.Asp301MetfsTer?
NM_001311257.1:c.853del	NP_001298186.1:p.Asp285MetfsTer?
XR_428840.2:n.945del
XR_428840.4:n.936del
NM_000506.5:c.901del MANE Select	NP_000497.1:p.Asp301MetfsTer?
NM_001311257.2:c.853del	NP_001298186.1:p.Asp285MetfsTer?