Canonical Allele Identifier: CA2695238174

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154905019del , CM000685.2:g.154905019del	GRCh38
NC_000023.10:g.154133294del , CM000685.1:g.154133294del	GRCh37
NC_000023.9:g.153786488del	NCBI36
NG_011403.1:g.122705del
NG_011403.2:g.122705del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5378del MANE Select	ENSP00000353393.4:p.Thr1793IlefsTer?
ENST00000360256.8:c.5378del	ENSP00000353393.4:p.Thr1793IlefsTer?
NM_000132.3:c.5378del	NP_000123.1:p.Thr1793IlefsTer?
XM_011531126.1:c.5273del	XP_011529428.1:p.Thr1758IlefsTer?
NM_000132.4:c.5378del MANE Select	NP_000123.1:p.Thr1793IlefsTer?