Canonical Allele Identifier: CA2613334381

Gene: F2

Linked Data

• gnomAD v4: 11-46725755-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725756dup , CM000673.2:g.46725756dup	GRCh38
NC_000011.9:g.46747306dup , CM000673.1:g.46747306dup	GRCh37
NC_000011.8:g.46703882dup	NCBI36
NG_008953.1:g.11564dup , LRG_551:g.11564dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.560-103dup MANE Select	ENSP00000308541.5:n.560-103dup
ENST00000311907.9:c.560-103dup	ENSP00000308541.5:n.560-103dup
ENST00000442468.1:c.530-103dup	ENSP00000387413.1:n.530-103dup
ENST00000490274.1:n.340-103dup
ENST00000530231.5:c.560-103dup	ENSP00000433907.1:n.560-103dup
NM_000506.3:c.560-103dup	NP_000497.1:n.560-103dup
NM_000506.4:c.560-103dup , LRG_551t1:c.560-103dup	NP_000497.1:n.560-103dup
NM_001311257.1:c.512-103dup	NP_001298186.1:n.512-103dup
XR_428840.2:n.604-103dup
XR_428840.4:n.595-103dup
NM_000506.5:c.560-103dup MANE Select	NP_000497.1:n.560-103dup
NM_001311257.2:c.512-103dup	NP_001298186.1:n.512-103dup