Canonical Allele Identifier: CA2824313402

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860359dup , CM000685.2:g.154860359dup	GRCh38
NC_000023.10:g.154088634dup , CM000685.1:g.154088634dup	GRCh37
NC_000023.9:g.153741828dup	NCBI36
NG_011403.1:g.167369dup
NG_011403.2:g.167369dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6900+77dup MANE Select	ENSP00000353393.4:n.6900+77dup
ENST00000644698.1:c.633+77dup	ENSP00000495706.1:n.633+77dup
ENST00000330287.10:c.495+77dup	ENSP00000327895.6:n.495+77dup
ENST00000360256.8:c.6900+77dup	ENSP00000353393.4:n.6900+77dup
NM_000132.3:c.6900+77dup	NP_000123.1:n.6900+77dup
NM_019863.2:c.495+77dup	NP_063916.1:n.495+77dup
XM_011531126.1:c.6795+77dup	XP_011529428.1:n.6795+77dup
NM_000132.4:c.6900+77dup MANE Select	NP_000123.1:n.6900+77dup
NM_019863.3:c.495+77dup	NP_063916.1:n.495+77dup