Canonical Allele Identifier: CA2613334382

Gene: F2

Linked Data

• gnomAD v4: 11-46725756-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725761_46725762del , CM000673.2:g.46725761_46725762del	GRCh38
NC_000011.9:g.46747311_46747312del , CM000673.1:g.46747311_46747312del	GRCh37
NC_000011.8:g.46703887_46703888del	NCBI36
NG_008953.1:g.11569_11570del , LRG_551:g.11569_11570del

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.560-98_560-97del MANE Select	ENSP00000308541.5:n.560-98_560-97del
ENST00000311907.9:c.560-98_560-97del	ENSP00000308541.5:n.560-98_560-97del
ENST00000442468.1:c.530-98_530-97del	ENSP00000387413.1:n.530-98_530-97del
ENST00000490274.1:n.340-98_340-97del
ENST00000530231.5:c.560-98_560-97del	ENSP00000433907.1:n.560-98_560-97del
NM_000506.3:c.560-98_560-97del	NP_000497.1:n.560-98_560-97del
NM_000506.4:c.560-98_560-97del , LRG_551t1:c.560-98_560-97del	NP_000497.1:n.560-98_560-97del
NM_001311257.1:c.512-98_512-97del	NP_001298186.1:n.512-98_512-97del
XR_428840.2:n.604-98_604-97del
XR_428840.4:n.595-98_595-97del
NM_000506.5:c.560-98_560-97del MANE Select	NP_000497.1:n.560-98_560-97del
NM_001311257.2:c.512-98_512-97del	NP_001298186.1:n.512-98_512-97del