Canonical Allele Identifier: CA2579744696

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154956905del , CM000685.2:g.154956905del	GRCh38
NC_000023.10:g.154185180del , CM000685.1:g.154185180del	GRCh37
NC_000023.9:g.153838374del	NCBI36
NG_011403.1:g.70820del
NG_011403.2:g.70820del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.1752+53del MANE Select	ENSP00000353393.4:n.1752+53del
ENST00000647125.1:c.*1628+53del	ENSP00000496062.1:n.*1628+53del
ENST00000360256.8:c.1752+53del	ENSP00000353393.4:n.1752+53del
NM_000132.3:c.1752+53del	NP_000123.1:n.1752+53del
XM_011531126.1:c.1647+53del	XP_011529428.1:n.1647+53del
NM_000132.4:c.1752+53del MANE Select	NP_000123.1:n.1752+53del