Canonical Allele Identifier: CA2695237949

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154903969del , CM000685.2:g.154903969del	GRCh38
NC_000023.10:g.154132244del , CM000685.1:g.154132244del	GRCh37
NC_000023.9:g.153785438del	NCBI36
NG_011403.1:g.123756del
NG_011403.2:g.123756del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5936del MANE Select	ENSP00000353393.4:p.Gly1979AspfsTer?
ENST00000360256.8:c.5936del	ENSP00000353393.4:p.Gly1979AspfsTer?
NM_000132.3:c.5936del	NP_000123.1:p.Gly1979AspfsTer?
XM_011531126.1:c.5831del	XP_011529428.1:p.Gly1944AspfsTer?
NM_000132.4:c.5936del MANE Select	NP_000123.1:p.Gly1979AspfsTer?