Canonical Allele Identifier: CA2579744569

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154905041_154905042del , CM000685.2:g.154905041_154905042del	GRCh38
NC_000023.10:g.154133316_154133317del , CM000685.1:g.154133316_154133317del	GRCh37
NC_000023.9:g.153786510_153786511del	NCBI36
NG_011403.1:g.122683_122684del
NG_011403.2:g.122683_122684del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5374-18_5374-17del MANE Select	ENSP00000353393.4:n.5374-18_5374-17del
ENST00000360256.8:c.5374-18_5374-17del	ENSP00000353393.4:n.5374-18_5374-17del
NM_000132.3:c.5374-18_5374-17del	NP_000123.1:n.5374-18_5374-17del
XM_011531126.1:c.5269-18_5269-17del	XP_011529428.1:n.5269-18_5269-17del
NM_000132.4:c.5374-18_5374-17del MANE Select	NP_000123.1:n.5374-18_5374-17del