Canonical Allele Identifier: CA2613334745

Gene: F2

Linked Data

• gnomAD v4: 11-46726178-GCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726179_46726180del , CM000673.2:g.46726179_46726180del	GRCh38
NC_000011.9:g.46747729_46747730del , CM000673.1:g.46747729_46747730del	GRCh37
NC_000011.8:g.46704305_46704306del	NCBI36
NG_008953.1:g.11987_11988del , LRG_551:g.11987_11988del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.874+6_874+7del MANE Select	ENSP00000308541.5:n.874+6_874+7del
ENST00000311907.9:c.874+6_874+7del	ENSP00000308541.5:n.874+6_874+7del
ENST00000442468.1:c.844+6_844+7del	ENSP00000387413.1:n.844+6_844+7del
ENST00000530231.5:c.874+6_874+7del	ENSP00000433907.1:n.874+6_874+7del
NM_000506.3:c.874+6_874+7del	NP_000497.1:n.874+6_874+7del
NM_000506.4:c.874+6_874+7del , LRG_551t1:c.874+6_874+7del	NP_000497.1:n.874+6_874+7del
NM_001311257.1:c.826+6_826+7del	NP_001298186.1:n.826+6_826+7del
XR_428840.2:n.918+6_918+7del
XR_428840.4:n.909+6_909+7del
NM_000506.5:c.874+6_874+7del MANE Select	NP_000497.1:n.874+6_874+7del
NM_001311257.2:c.826+6_826+7del	NP_001298186.1:n.826+6_826+7del