Canonical Allele Identifier: CA873367304

Gene: F8

Linked Data

• dbSNP Id: rs1453026332
• MyVariant Identifiers: chrX:g.155022446_155022457del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022446_155022457del , CM000685.2:g.155022446_155022457del	GRCh38
NC_000023.10:g.154250721_154250732del , CM000685.1:g.154250721_154250732del	GRCh37
NC_000023.9:g.153903915_153903926del	NCBI36
NG_011403.1:g.5267_5278del
NG_011403.2:g.5267_5278del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.96_107del MANE Select	ENSP00000353393.4:p.Trp33_Met36del
ENST00000647125.1:c.96_107del	ENSP00000496062.1:p.Trp33_Met36del
ENST00000360256.8:c.96_107del	ENSP00000353393.4:p.Trp33_Met36del
ENST00000423959.5:c.38+4323_38+4334del	ENSP00000409446.1:n.38+4323_38+4334del
ENST00000453950.1:c.78_89del	ENSP00000389153.1:p.Trp27_Met30del
NM_000132.3:c.96_107del	NP_000123.1:p.Trp33_Met36del
XM_011531126.1:c.38+4323_38+4334del	XP_011529428.1:n.38+4323_38+4334del
NM_000132.4:c.96_107del MANE Select	NP_000123.1:p.Trp33_Met36del