Canonical Allele Identifier: CA2613334788

Gene: F2

Linked Data

• gnomAD v4: 11-46726189-A-AGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726193_46726194dup , CM000673.2:g.46726193_46726194dup	GRCh38
NC_000011.9:g.46747743_46747744dup , CM000673.1:g.46747743_46747744dup	GRCh37
NC_000011.8:g.46704319_46704320dup	NCBI36
NG_008953.1:g.12001_12002dup , LRG_551:g.12001_12002dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.874+20_874+21dup MANE Select	ENSP00000308541.5:n.874+20_874+21dup
ENST00000311907.9:c.874+20_874+21dup	ENSP00000308541.5:n.874+20_874+21dup
ENST00000442468.1:c.844+20_844+21dup	ENSP00000387413.1:n.844+20_844+21dup
ENST00000530231.5:c.874+20_874+21dup	ENSP00000433907.1:n.874+20_874+21dup
NM_000506.3:c.874+20_874+21dup	NP_000497.1:n.874+20_874+21dup
NM_000506.4:c.874+20_874+21dup , LRG_551t1:c.874+20_874+21dup	NP_000497.1:n.874+20_874+21dup
NM_001311257.1:c.826+20_826+21dup	NP_001298186.1:n.826+20_826+21dup
XR_428840.2:n.918+20_918+21dup
XR_428840.4:n.909+20_909+21dup
NM_000506.5:c.874+20_874+21dup MANE Select	NP_000497.1:n.874+20_874+21dup
NM_001311257.2:c.826+20_826+21dup	NP_001298186.1:n.826+20_826+21dup