Canonical Allele Identifier: CA2695237131

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860531del , CM000685.2:g.154860531del	GRCh38
NC_000023.10:g.154088806del , CM000685.1:g.154088806del	GRCh37
NC_000023.9:g.153742000del	NCBI36
NG_011403.1:g.167196del
NG_011403.2:g.167196del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6804del MANE Select	ENSP00000353393.4:p.Lys2268AsnfsTer9
ENST00000644698.1:c.537del	ENSP00000495706.1:p.Lys179AsnfsTer9
ENST00000330287.10:c.399del	ENSP00000327895.6:p.Lys133AsnfsTer9
ENST00000360256.8:c.6804del	ENSP00000353393.4:p.Lys2268AsnfsTer9
NM_000132.3:c.6804del	NP_000123.1:p.Lys2268AsnfsTer9
NM_019863.2:c.399del	NP_063916.1:p.Lys133AsnfsTer9
XM_011531126.1:c.6699del	XP_011529428.1:p.Lys2233AsnfsTer9
NM_000132.4:c.6804del MANE Select	NP_000123.1:p.Lys2268AsnfsTer9
NM_019863.3:c.399del	NP_063916.1:p.Lys133AsnfsTer9