Canonical Allele Identifier: CA645251868

Gene: F8

Linked Data

• dbSNP Id: rs1557287565
• gnomAD v2: X-154250568-TC-T
• gnomAD v3: X-155022293-TC-T
• gnomAD v4: X-155022293-TC-T
• MyVariant Identifiers: chrX:g.154250569del (hg19) ; chrX:g.155022294del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022294del , CM000685.2:g.155022294del	GRCh38
NC_000023.10:g.154250569del , CM000685.1:g.154250569del	GRCh37
NC_000023.9:g.153903763del	NCBI36
NG_011403.1:g.5430del
NG_011403.2:g.5430del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.143+116del MANE Select	ENSP00000353393.4:n.143+116del
ENST00000647125.1:c.121+138del	ENSP00000496062.1:n.121+138del
ENST00000360256.8:c.143+116del	ENSP00000353393.4:n.143+116del
ENST00000423959.5:c.38+4486del	ENSP00000409446.1:n.38+4486del
ENST00000453950.1:c.125+116del	ENSP00000389153.1:n.125+116del
NM_000132.3:c.143+116del	NP_000123.1:n.143+116del
XM_011531126.1:c.38+4486del	XP_011529428.1:n.38+4486del
NM_000132.4:c.143+116del MANE Select	NP_000123.1:n.143+116del