Canonical Allele Identifier: CA2579744571

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154905067_154905069del , CM000685.2:g.154905067_154905069del	GRCh38
NC_000023.10:g.154133342_154133344del , CM000685.1:g.154133342_154133344del	GRCh37
NC_000023.9:g.153786536_153786538del	NCBI36
NG_011403.1:g.122658_122660del
NG_011403.2:g.122658_122660del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5374-43_5374-41del MANE Select	ENSP00000353393.4:n.5374-43_5374-41del
ENST00000360256.8:c.5374-43_5374-41del	ENSP00000353393.4:n.5374-43_5374-41del
NM_000132.3:c.5374-43_5374-41del	NP_000123.1:n.5374-43_5374-41del
XM_011531126.1:c.5269-43_5269-41del	XP_011529428.1:n.5269-43_5269-41del
NM_000132.4:c.5374-43_5374-41del MANE Select	NP_000123.1:n.5374-43_5374-41del