Canonical Allele Identifier: CA2824314807

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154901957dup , CM000685.2:g.154901957dup	GRCh38
NC_000023.10:g.154130232dup , CM000685.1:g.154130232dup	GRCh37
NC_000023.9:g.153783426dup	NCBI36
NG_011403.1:g.125769dup
NG_011403.2:g.125769dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6115+96dup MANE Select	ENSP00000353393.4:n.6115+96dup
ENST00000360256.8:c.6115+96dup	ENSP00000353393.4:n.6115+96dup
NM_000132.3:c.6115+96dup	NP_000123.1:n.6115+96dup
XM_011531126.1:c.6010+96dup	XP_011529428.1:n.6010+96dup
NM_000132.4:c.6115+96dup MANE Select	NP_000123.1:n.6115+96dup