Canonical Allele Identifier: CA2466856537

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154993048_154993049delinsAT , CM000685.2:g.154993048_154993049delinsAT	GRCh38
NC_000023.10:g.154221323_154221324delinsAT , CM000685.1:g.154221323_154221324delinsAT	GRCh37
NC_000023.9:g.153874517_153874518delinsAT	NCBI36
NG_011403.1:g.34675_34676delinsAT
NG_011403.2:g.34675_34676delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.488_489delinsAT MANE Select	ENSP00000353393.4:p.Asn163=
ENST00000647125.1:c.*274_*275delinsAT	ENSP00000496062.1:n.*274_*275delinsAT
ENST00000360256.8:c.488_489delinsAT	ENSP00000353393.4:p.Asn163=
ENST00000423959.5:c.383_384delinsAT	ENSP00000409446.1:p.Asn128=
ENST00000453950.1:c.470_471delinsAT	ENSP00000389153.1:p.Asn157=
NM_000132.3:c.488_489delinsAT	NP_000123.1:p.Asn163=
XM_011531126.1:c.383_384delinsAT	XP_011529428.1:p.Asn128=
NM_000132.4:c.488_489delinsAT MANE Select	NP_000123.1:p.Asn163=