Canonical Allele Identifier: CA2695237180

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863195del , CM000685.2:g.154863195del	GRCh38
NC_000023.10:g.154091470del , CM000685.1:g.154091470del	GRCh37
NC_000023.9:g.153744664del	NCBI36
NG_011403.1:g.164532del
NG_011403.2:g.164532del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6465del MANE Select	ENSP00000353393.4:p.Lys2155AsnfsTer?
ENST00000644698.1:c.198del	ENSP00000495706.1:p.Lys66AsnfsTer?
ENST00000330287.10:c.60del	ENSP00000327895.6:p.Lys20AsnfsTer?
ENST00000360256.8:c.6465del	ENSP00000353393.4:p.Lys2155AsnfsTer?
NM_000132.3:c.6465del	NP_000123.1:p.Lys2155AsnfsTer?
NM_019863.2:c.60del	NP_063916.1:p.Lys20AsnfsTer?
XM_011531126.1:c.6360del	XP_011529428.1:p.Lys2120AsnfsTer?
NM_000132.4:c.6465del MANE Select	NP_000123.1:p.Lys2155AsnfsTer?
NM_019863.3:c.60del	NP_063916.1:p.Lys20AsnfsTer?