Canonical Allele Identifier: CA2695238942

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022482_155022483insGGCACTAAAGC , CM000685.2:g.155022482_155022483insGGCACTAAAGC	GRCh38
NC_000023.10:g.154250757_154250758insGGCACTAAAGC , CM000685.1:g.154250757_154250758insGGCACTAAAGC	GRCh37
NC_000023.9:g.153903951_153903952insGGCACTAAAGC	NCBI36
NG_011403.1:g.5241_5242insGCTTTAGTGCC
NG_011403.2:g.5241_5242insGCTTTAGTGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.70_71insGCTTTAGTGCC MANE Select	ENSP00000353393.4:p.Tyr24CysfsTer?
ENST00000647125.1:c.70_71insGCTTTAGTGCC	ENSP00000496062.1:p.Tyr24CysfsTer25
ENST00000360256.8:c.70_71insGCTTTAGTGCC	ENSP00000353393.4:p.Tyr24CysfsTer?
ENST00000423959.5:c.38+4297_38+4298insGCTTTAGTGCC	ENSP00000409446.1:n.38+4297_38+4298insGCTTTAGTGCC
ENST00000453950.1:c.52_53insGCTTTAGTGCC	ENSP00000389153.1:p.Tyr18CysfsTer?
NM_000132.3:c.70_71insGCTTTAGTGCC	NP_000123.1:p.Tyr24CysfsTer?
XM_011531126.1:c.38+4297_38+4298insGCTTTAGTGCC	XP_011529428.1:n.38+4297_38+4298insGCTTTAGTGCC
NM_000132.4:c.70_71insGCTTTAGTGCC MANE Select	NP_000123.1:p.Tyr24CysfsTer?