Canonical Allele Identifier: CA2579753317

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022318dup , CM000685.2:g.155022318dup	GRCh38
NC_000023.10:g.154250593dup , CM000685.1:g.154250593dup	GRCh37
NC_000023.9:g.153903787dup	NCBI36
NG_011403.1:g.5407dup
NG_011403.2:g.5407dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.143+93dup MANE Select	ENSP00000353393.4:n.143+93dup
ENST00000647125.1:c.121+115dup	ENSP00000496062.1:n.121+115dup
ENST00000360256.8:c.143+93dup	ENSP00000353393.4:n.143+93dup
ENST00000423959.5:c.38+4463dup	ENSP00000409446.1:n.38+4463dup
ENST00000453950.1:c.125+93dup	ENSP00000389153.1:n.125+93dup
NM_000132.3:c.143+93dup	NP_000123.1:n.143+93dup
XM_011531126.1:c.38+4463dup	XP_011529428.1:n.38+4463dup
NM_000132.4:c.143+93dup MANE Select	NP_000123.1:n.143+93dup