Canonical Allele Identifier: CA2695237119

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860434_154860435dup , CM000685.2:g.154860434_154860435dup	GRCh38
NC_000023.10:g.154088709_154088710dup , CM000685.1:g.154088709_154088710dup	GRCh37
NC_000023.9:g.153741903_153741904dup	NCBI36
NG_011403.1:g.167290_167291dup
NG_011403.2:g.167290_167291dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6898_6899dup MANE Select	ENSP00000353393.4:p.Val2301ArgfsTer14
ENST00000644698.1:c.631_632dup	ENSP00000495706.1:p.Val212ArgfsTer14
ENST00000330287.10:c.493_494dup	ENSP00000327895.6:p.Val166ArgfsTer14
ENST00000360256.8:c.6898_6899dup	ENSP00000353393.4:p.Val2301ArgfsTer14
NM_000132.3:c.6898_6899dup	NP_000123.1:p.Val2301ArgfsTer14
NM_019863.2:c.493_494dup	NP_063916.1:p.Val166ArgfsTer14
XM_011531126.1:c.6793_6794dup	XP_011529428.1:p.Val2266ArgfsTer14
NM_000132.4:c.6898_6899dup MANE Select	NP_000123.1:p.Val2301ArgfsTer14
NM_019863.3:c.493_494dup	NP_063916.1:p.Val166ArgfsTer14