Canonical Allele Identifier: CA2574810761

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46723362del , CM000673.2:g.46723362del	GRCh38
NC_000011.9:g.46744912del , CM000673.1:g.46744912del	GRCh37
NC_000011.8:g.46701488del	NCBI36
NG_008953.1:g.9170del , LRG_551:g.9170del

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.423-20del MANE Select	ENSP00000308541.5:n.423-20del
ENST00000311907.9:c.423-20del	ENSP00000308541.5:n.423-20del
ENST00000442468.1:c.393-20del	ENSP00000387413.1:n.393-20del
ENST00000490274.1:n.183del
ENST00000530231.5:c.423-20del	ENSP00000433907.1:n.423-20del
NM_000506.3:c.423-20del	NP_000497.1:n.423-20del
NM_000506.4:c.423-20del , LRG_551t1:c.423-20del	NP_000497.1:n.423-20del
NM_001311257.1:c.375-20del	NP_001298186.1:n.375-20del
XR_428840.2:n.467-20del
XR_428840.4:n.458-20del
NM_000506.5:c.423-20del MANE Select	NP_000497.1:n.423-20del
NM_001311257.2:c.375-20del	NP_001298186.1:n.375-20del