Canonical Allele Identifier: CA2574810785

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725791_46725792del , CM000673.2:g.46725791_46725792del	GRCh38
NC_000011.9:g.46747341_46747342del , CM000673.1:g.46747341_46747342del	GRCh37
NC_000011.8:g.46703917_46703918del	NCBI36
NG_008953.1:g.11599_11600del , LRG_551:g.11599_11600del

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.560-68_560-67del MANE Select	ENSP00000308541.5:n.560-68_560-67del
ENST00000311907.9:c.560-68_560-67del	ENSP00000308541.5:n.560-68_560-67del
ENST00000442468.1:c.530-68_530-67del	ENSP00000387413.1:n.530-68_530-67del
ENST00000490274.1:n.340-68_340-67del
ENST00000530231.5:c.560-68_560-67del	ENSP00000433907.1:n.560-68_560-67del
NM_000506.3:c.560-68_560-67del	NP_000497.1:n.560-68_560-67del
NM_000506.4:c.560-68_560-67del , LRG_551t1:c.560-68_560-67del	NP_000497.1:n.560-68_560-67del
NM_001311257.1:c.512-68_512-67del	NP_001298186.1:n.512-68_512-67del
XR_428840.2:n.604-68_604-67del
XR_428840.4:n.595-68_595-67del
NM_000506.5:c.560-68_560-67del MANE Select	NP_000497.1:n.560-68_560-67del
NM_001311257.2:c.512-68_512-67del	NP_001298186.1:n.512-68_512-67del