Canonical Allele Identifier: CA2466865415

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022445_155022457delinsCATATAGTCCCAT , CM000685.2:g.155022445_155022457delinsCATATAGTCCCAT	GRCh38
NC_000023.10:g.154250720_154250732delinsCATATAGTCCCAT , CM000685.1:g.154250720_154250732delinsCATATAGTCCCAT	GRCh37
NC_000023.9:g.153903914_153903926delinsCATATAGTCCCAT	NCBI36
NG_011403.1:g.5267_5279delinsATGGGACTATATG
NG_011403.2:g.5267_5279delinsATGGGACTATATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.96_108delinsATGGGACTATATG MANE Select	ENSP00000353393.4:p.Ser32=
ENST00000647125.1:c.96_108delinsATGGGACTATATG	ENSP00000496062.1:p.Ser32=
ENST00000360256.8:c.96_108delinsATGGGACTATATG	ENSP00000353393.4:p.Ser32=
ENST00000423959.5:c.38+4323_38+4335delinsATGGGACTATATG	ENSP00000409446.1:n.38+4323_38+4335delinsATGGGACTATATG
ENST00000453950.1:c.78_90delinsATGGGACTATATG	ENSP00000389153.1:p.Ser26=
NM_000132.3:c.96_108delinsATGGGACTATATG	NP_000123.1:p.Ser32=
XM_011531126.1:c.38+4323_38+4335delinsATGGGACTATATG	XP_011529428.1:n.38+4323_38+4335delinsATGGGACTATATG
NM_000132.4:c.96_108delinsATGGGACTATATG MANE Select	NP_000123.1:p.Ser32=