Canonical Allele Identifier: CA2613334393

Gene: F2

Linked Data

• gnomAD v4: 11-46725769-AAGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725774_46725776del , CM000673.2:g.46725774_46725776del	GRCh38
NC_000011.9:g.46747324_46747326del , CM000673.1:g.46747324_46747326del	GRCh37
NC_000011.8:g.46703900_46703902del	NCBI36
NG_008953.1:g.11582_11584del , LRG_551:g.11582_11584del

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.560-85_560-83del MANE Select	ENSP00000308541.5:n.560-85_560-83del
ENST00000311907.9:c.560-85_560-83del	ENSP00000308541.5:n.560-85_560-83del
ENST00000442468.1:c.530-85_530-83del	ENSP00000387413.1:n.530-85_530-83del
ENST00000490274.1:n.340-85_340-83del
ENST00000530231.5:c.560-85_560-83del	ENSP00000433907.1:n.560-85_560-83del
NM_000506.3:c.560-85_560-83del	NP_000497.1:n.560-85_560-83del
NM_000506.4:c.560-85_560-83del , LRG_551t1:c.560-85_560-83del	NP_000497.1:n.560-85_560-83del
NM_001311257.1:c.512-85_512-83del	NP_001298186.1:n.512-85_512-83del
XR_428840.2:n.604-85_604-83del
XR_428840.4:n.595-85_595-83del
NM_000506.5:c.560-85_560-83del MANE Select	NP_000497.1:n.560-85_560-83del
NM_001311257.2:c.512-85_512-83del	NP_001298186.1:n.512-85_512-83del