Canonical Allele Identifier: CA2536973539

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997065del , CM000685.2:g.154997065del	GRCh38
NC_000023.10:g.154225340del , CM000685.1:g.154225340del	GRCh37
NC_000023.9:g.153878534del	NCBI36
NG_011403.1:g.30661del
NG_011403.2:g.30661del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.298del MANE Select	ENSP00000353393.4:p.Tyr100MetfsTer?
ENST00000647125.1:c.*84del	ENSP00000496062.1:n.*84del
ENST00000360256.8:c.298del	ENSP00000353393.4:p.Tyr100MetfsTer?
ENST00000423959.5:c.193del	ENSP00000409446.1:p.Tyr65MetfsTer?
ENST00000453950.1:c.280del	ENSP00000389153.1:p.Tyr94MetfsTer?
NM_000132.3:c.298del	NP_000123.1:p.Tyr100MetfsTer?
XM_011531126.1:c.193del	XP_011529428.1:p.Tyr65MetfsTer?
NM_000132.4:c.298del MANE Select	NP_000123.1:p.Tyr100MetfsTer?