Canonical Allele Identifier: CA2695237816

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896075del , CM000685.2:g.154896075del	GRCh38
NC_000023.10:g.154124350del , CM000685.1:g.154124350del	GRCh37
NC_000023.9:g.153777544del	NCBI36
NG_011403.1:g.131649del
NG_011403.2:g.131649del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6429+2del MANE Select	ENSP00000353393.4:n.6429+2del
ENST00000360256.8:c.6429+2del	ENSP00000353393.4:n.6429+2del
NM_000132.3:c.6429+2del	NP_000123.1:n.6429+2del
XM_011531126.1:c.6324+2del	XP_011529428.1:n.6324+2del
NM_000132.4:c.6429+2del MANE Select	NP_000123.1:n.6429+2del