Canonical Allele Identifier: CA599372329

Gene: F2

Linked Data

• dbSNP Id: rs1565703706
• gnomAD v2: 11-46747730-TGCCTGGGTAGGGG-T
• gnomAD v4: 11-46726180-TGCCTGGGTAGGGG-T
• MyVariant Identifiers: chr11:g.46747731_46747743del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726186_46726198del , CM000673.2:g.46726186_46726198del	GRCh38
NC_000011.9:g.46747736_46747748del , CM000673.1:g.46747736_46747748del	GRCh37
NC_000011.8:g.46704312_46704324del	NCBI36
NG_008953.1:g.11994_12006del , LRG_551:g.11994_12006del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.874+13_874+25del MANE Select	ENSP00000308541.5:n.874+13_874+25del
ENST00000311907.9:c.874+13_874+25del	ENSP00000308541.5:n.874+13_874+25del
ENST00000442468.1:c.844+13_844+25del	ENSP00000387413.1:n.844+13_844+25del
ENST00000530231.5:c.874+13_874+25del	ENSP00000433907.1:n.874+13_874+25del
NM_000506.3:c.874+13_874+25del	NP_000497.1:n.874+13_874+25del
NM_000506.4:c.874+13_874+25del , LRG_551t1:c.874+13_874+25del	NP_000497.1:n.874+13_874+25del
NM_001311257.1:c.826+13_826+25del	NP_001298186.1:n.826+13_826+25del
XR_428840.2:n.918+13_918+25del
XR_428840.4:n.909+13_909+25del
NM_000506.5:c.874+13_874+25del MANE Select	NP_000497.1:n.874+13_874+25del
NM_001311257.2:c.826+13_826+25del	NP_001298186.1:n.826+13_826+25del