Canonical Allele Identifier: CA1969073815

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46727840_46727857delinsTCCAGGCCCCAAAGGCGG , CM000673.2:g.46727840_46727857delinsTCCAGGCCCCAAAGGCGG	GRCh38
NC_000011.9:g.46749390_46749407delinsTCCAGGCCCCAAAGGCGG , CM000673.1:g.46749390_46749407delinsTCCAGGCCCCAAAGGCGG	GRCh37
NC_000011.8:g.46705966_46705983delinsTCCAGGCCCCAAAGGCGG	NCBI36
NG_008953.1:g.13648_13665delinsTCCAGGCCCCAAAGGCGG , LRG_551:g.13648_13665delinsTCCAGGCCCCAAAGGCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1131-156_1131-139delinsTCCAGGCCCCAAAGGCGG MANE Select	ENSP00000308541.5:n.1131-156_1131-139delinsTCCAGGCCCCAAAGGCGG...
ENST00000311907.9:c.1131-156_1131-139delinsTCCAGGCCCCAAAGGCGG	ENSP00000308541.5:n.1131-156_1131-139delinsTCCAGGCCCCAAAGGCGG...
ENST00000530231.5:c.1131-156_1131-139delinsTCCAGGCCCCAAAGGCGG	ENSP00000433907.1:n.1131-156_1131-139delinsTCCAGGCCCCAAAGGCGG...
NM_000506.3:c.1131-156_1131-139delinsTCCAGGCCCCAAAGGCGG	NP_000497.1:n.1131-156_1131-139delinsTCCAGGCCCCAAAGGCGG
NM_000506.4:c.1131-156_1131-139delinsTCCAGGCCCCAAAGGCGG , LRG_551t1:c.1131-156_1131-139delinsTCCAGGCCCCAAAGGCGG	NP_000497.1:n.1131-156_1131-139delinsTCCAGGCCCCAAAGGCGG
NM_001311257.1:c.1083-156_1083-139delinsTCCAGGCCCCAAAGGCGG	NP_001298186.1:n.1083-156_1083-139delinsTCCAGGCCCCAAAGGCGG
XR_428840.2:n.1175-156_1175-139delinsTCCAGGCCCCAAAGGCGG
XR_428840.4:n.1166-156_1166-139delinsTCCAGGCCCCAAAGGCGG
NM_000506.5:c.1131-156_1131-139delinsTCCAGGCCCCAAAGGCGG MANE Select	NP_000497.1:n.1131-156_1131-139delinsTCCAGGCCCCAAAGGCGG
NM_001311257.2:c.1083-156_1083-139delinsTCCAGGCCCCAAAGGCGG	NP_001298186.1:n.1083-156_1083-139delinsTCCAGGCCCCAAAGGCGG