Canonical Allele Identifier: CA873368334

Gene: F8

Linked Data

• dbSNP Id: rs1405834091
• MyVariant Identifiers: chrX:g.154860503_154860504insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860504dup , CM000685.2:g.154860504dup	GRCh38
NC_000023.10:g.154088779dup , CM000685.1:g.154088779dup	GRCh37
NC_000023.9:g.153741973dup	NCBI36
NG_011403.1:g.167220dup
NG_011403.2:g.167220dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6828dup MANE Select	ENSP00000353393.4:p.Lys2277GlufsTer?
ENST00000644698.1:c.561dup	ENSP00000495706.1:p.Lys188GlufsTer?
ENST00000330287.10:c.423dup	ENSP00000327895.6:p.Lys142GlufsTer?
ENST00000360256.8:c.6828dup	ENSP00000353393.4:p.Lys2277GlufsTer?
NM_000132.3:c.6828dup	NP_000123.1:p.Lys2277GlufsTer?
NM_019863.2:c.423dup	NP_063916.1:p.Lys142GlufsTer?
XM_011531126.1:c.6723dup	XP_011529428.1:p.Lys2242GlufsTer?
NM_000132.4:c.6828dup MANE Select	NP_000123.1:p.Lys2277GlufsTer?
NM_019863.3:c.423dup	NP_063916.1:p.Lys142GlufsTer?