Canonical Allele Identifier: CA873367490

Gene: F8

Linked Data

• dbSNP Id: rs1321981494
• gnomAD v3: X-155022523-AAAG-A
• gnomAD v4: X-155022523-AAAG-A
• MyVariant Identifiers: chrX:g.155022524_155022526del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022527_155022529del , CM000685.2:g.155022527_155022529del	GRCh38
NC_000023.10:g.154250802_154250804del , CM000685.1:g.154250802_154250804del	GRCh37
NC_000023.9:g.153903996_153903998del	NCBI36
NG_011403.1:g.5198_5200del
NG_011403.2:g.5198_5200del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.27_29del MANE Select	ENSP00000353393.4:p.Phe10del
ENST00000647125.1:c.27_29del	ENSP00000496062.1:p.Phe10del
ENST00000360256.8:c.27_29del	ENSP00000353393.4:p.Phe10del
ENST00000423959.5:c.38+4254_38+4256del	ENSP00000409446.1:n.38+4254_38+4256del
ENST00000453950.1:c.39-30_39-28del	ENSP00000389153.1:n.39-30_39-28del
NM_000132.3:c.27_29del	NP_000123.1:p.Phe10del
XM_011531126.1:c.38+4254_38+4256del	XP_011529428.1:n.38+4254_38+4256del
NM_000132.4:c.27_29del MANE Select	NP_000123.1:p.Phe10del