Canonical Allele Identifier: CA2695237836

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896211del , CM000685.2:g.154896211del	GRCh38
NC_000023.10:g.154124486del , CM000685.1:g.154124486del	GRCh37
NC_000023.9:g.153777680del	NCBI36
NG_011403.1:g.131513del
NG_011403.2:g.131513del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6295del MANE Select	ENSP00000353393.4:p.Ile2099LeufsTer?
ENST00000360256.8:c.6295del	ENSP00000353393.4:p.Ile2099LeufsTer?
NM_000132.3:c.6295del	NP_000123.1:p.Ile2099LeufsTer?
XM_011531126.1:c.6190del	XP_011529428.1:p.Ile2064LeufsTer?
NM_000132.4:c.6295del MANE Select	NP_000123.1:p.Ile2099LeufsTer?