Canonical Allele Identifier: CA2695237249

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154956954dup , CM000685.2:g.154956954dup	GRCh38
NC_000023.10:g.154185229dup , CM000685.1:g.154185229dup	GRCh37
NC_000023.9:g.153838423dup	NCBI36
NG_011403.1:g.70770dup
NG_011403.2:g.70770dup

Transcript Alleles

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