Canonical Allele Identifier: CA1969072366

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726180_46726193delinsTGCCTGGGTAGGGG , CM000673.2:g.46726180_46726193delinsTGCCTGGGTAGGGG	GRCh38
NC_000011.9:g.46747730_46747743delinsTGCCTGGGTAGGGG , CM000673.1:g.46747730_46747743delinsTGCCTGGGTAGGGG	GRCh37
NC_000011.8:g.46704306_46704319delinsTGCCTGGGTAGGGG	NCBI36
NG_008953.1:g.11988_12001delinsTGCCTGGGTAGGGG , LRG_551:g.11988_12001delinsTGCCTGGGTAGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.874+7_874+20delinsTGCCTGGGTAGGGG MANE Select	ENSP00000308541.5:n.874+7_874+20delinsTGCCTGGGTAGGGG
ENST00000311907.9:c.874+7_874+20delinsTGCCTGGGTAGGGG	ENSP00000308541.5:n.874+7_874+20delinsTGCCTGGGTAGGGG
ENST00000442468.1:c.844+7_844+20delinsTGCCTGGGTAGGGG	ENSP00000387413.1:n.844+7_844+20delinsTGCCTGGGTAGGGG
ENST00000530231.5:c.874+7_874+20delinsTGCCTGGGTAGGGG	ENSP00000433907.1:n.874+7_874+20delinsTGCCTGGGTAGGGG
NM_000506.3:c.874+7_874+20delinsTGCCTGGGTAGGGG	NP_000497.1:n.874+7_874+20delinsTGCCTGGGTAGGGG
NM_000506.4:c.874+7_874+20delinsTGCCTGGGTAGGGG , LRG_551t1:c.874+7_874+20delinsTGCCTGGGTAGGGG	NP_000497.1:n.874+7_874+20delinsTGCCTGGGTAGGGG
NM_001311257.1:c.826+7_826+20delinsTGCCTGGGTAGGGG	NP_001298186.1:n.826+7_826+20delinsTGCCTGGGTAGGGG
XR_428840.2:n.918+7_918+20delinsTGCCTGGGTAGGGG
XR_428840.4:n.909+7_909+20delinsTGCCTGGGTAGGGG
NM_000506.5:c.874+7_874+20delinsTGCCTGGGTAGGGG MANE Select	NP_000497.1:n.874+7_874+20delinsTGCCTGGGTAGGGG
NM_001311257.2:c.826+7_826+20delinsTGCCTGGGTAGGGG	NP_001298186.1:n.826+7_826+20delinsTGCCTGGGTAGGGG