Canonical Allele Identifier: CA873350209

Gene: F8

Linked Data

• dbSNP Id: rs1366142523
• MyVariant Identifiers: chrX:g.154947752_154947753del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154947756_154947757del , CM000685.2:g.154947756_154947757del	GRCh38
NC_000023.10:g.154176031_154176032del , CM000685.1:g.154176031_154176032del	GRCh37
NC_000023.9:g.153829225_153829226del	NCBI36
NG_011403.1:g.79971_79972del
NG_011403.2:g.79971_79972del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.2058_2059del MANE Select	ENSP00000353393.4:p.Leu687HisfsTer?
ENST00000647125.1:c.*1779+6139_*1779+6140del	ENSP00000496062.1:n.*1779+6139_*1779+6140...
ENST00000360256.8:c.2058_2059del	ENSP00000353393.4:p.Leu687HisfsTer?
NM_000132.3:c.2058_2059del	NP_000123.1:p.Leu687HisfsTer?
XM_011531126.1:c.1953_1954del	XP_011529428.1:p.Leu652HisfsTer?
NM_000132.4:c.2058_2059del MANE Select	NP_000123.1:p.Leu687HisfsTer?