Canonical Allele Identifier: CA2838572530

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154956892dup , CM000685.2:g.154956892dup	GRCh38
NC_000023.10:g.154185167dup , CM000685.1:g.154185167dup	GRCh37
NC_000023.9:g.153838361dup	NCBI36
NG_011403.1:g.70835dup
NG_011403.2:g.70835dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1752+68dup MANE Select	ENSP00000353393.4:n.1752+68dup
ENST00000647125.1:c.*1628+68dup	ENSP00000496062.1:n.*1628+68dup
ENST00000360256.8:c.1752+68dup	ENSP00000353393.4:n.1752+68dup
NM_000132.3:c.1752+68dup	NP_000123.1:n.1752+68dup
XM_011531126.1:c.1647+68dup	XP_011529428.1:n.1647+68dup
NM_000132.4:c.1752+68dup MANE Select	NP_000123.1:n.1752+68dup