Canonical Allele Identifier: CA2695238545

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022541del , CM000685.2:g.155022541del	GRCh38
NC_000023.10:g.154250816del , CM000685.1:g.154250816del	GRCh37
NC_000023.9:g.153904010del	NCBI36
NG_011403.1:g.5183del
NG_011403.2:g.5183del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.12del MANE Select	ENSP00000353393.4:p.Glu4AspfsTer?
ENST00000647125.1:c.12del	ENSP00000496062.1:p.Glu4AspfsTer?
ENST00000360256.8:c.12del	ENSP00000353393.4:p.Glu4AspfsTer?
ENST00000423959.5:c.38+4239del	ENSP00000409446.1:n.38+4239del
ENST00000453950.1:c.39-45del	ENSP00000389153.1:n.39-45del
NM_000132.3:c.12del	NP_000123.1:p.Glu4AspfsTer?
XM_011531126.1:c.38+4239del	XP_011529428.1:n.38+4239del
NM_000132.4:c.12del MANE Select	NP_000123.1:p.Glu4AspfsTer?