Canonical Allele Identifier: CA2824314887

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154905057del , CM000685.2:g.154905057del	GRCh38
NC_000023.10:g.154133332del , CM000685.1:g.154133332del	GRCh37
NC_000023.9:g.153786526del	NCBI36
NG_011403.1:g.122668del
NG_011403.2:g.122668del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5374-33del MANE Select	ENSP00000353393.4:n.5374-33del
ENST00000360256.8:c.5374-33del	ENSP00000353393.4:n.5374-33del
NM_000132.3:c.5374-33del	NP_000123.1:n.5374-33del
XM_011531126.1:c.5269-33del	XP_011529428.1:n.5269-33del
NM_000132.4:c.5374-33del MANE Select	NP_000123.1:n.5374-33del