Canonical Allele Identifier: CA2695237106

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837660dup , CM000685.2:g.154837660dup	GRCh38
NC_000023.10:g.154065935dup , CM000685.1:g.154065935dup	GRCh37
NC_000023.9:g.153719129dup	NCBI36
NG_011403.1:g.190065dup
NG_033065.1:g.2004dup
NG_011403.2:g.190065dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6994dup MANE Select	ENSP00000353393.4:p.Trp2332LeufsTer?
ENST00000644698.1:c.727dup	ENSP00000495706.1:p.Trp243LeufsTer?
ENST00000330287.10:c.589dup	ENSP00000327895.6:p.Trp197LeufsTer?
ENST00000360256.8:c.6994dup	ENSP00000353393.4:p.Trp2332LeufsTer?
NM_000132.3:c.6994dup	NP_000123.1:p.Trp2332LeufsTer?
NM_019863.2:c.589dup	NP_063916.1:p.Trp197LeufsTer?
XM_011531126.1:c.6889dup	XP_011529428.1:p.Trp2297LeufsTer?
NM_000132.4:c.6994dup MANE Select	NP_000123.1:p.Trp2332LeufsTer?
NM_019863.3:c.589dup	NP_063916.1:p.Trp197LeufsTer?