Canonical Allele Identifier: CA873352669

Gene: F8

Linked Data

• dbSNP Id: rs1316272027
• gnomAD v3: X-154954331-G-GTCTGTAGC
• gnomAD v4: X-154954331-G-GTCTGTAGC
• MyVariant Identifiers: chrX:g.154954331_154954332insTCTGTAGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154954332_154954339dup , CM000685.2:g.154954332_154954339dup	GRCh38
NC_000023.10:g.154182607_154182614dup , CM000685.1:g.154182607_154182614dup	GRCh37
NC_000023.9:g.153835801_153835808dup	NCBI36
NG_011403.1:g.73385_73392dup
NG_011403.2:g.73385_73392dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1753-297_1753-290dup MANE Select	ENSP00000353393.4:n.1753-297_1753-290dup
ENST00000647125.1:c.*1629-297_*1629-290dup	ENSP00000496062.1:n.*1629-297_*1629-290dup
ENST00000360256.8:c.1753-297_1753-290dup	ENSP00000353393.4:n.1753-297_1753-290dup
NM_000132.3:c.1753-297_1753-290dup	NP_000123.1:n.1753-297_1753-290dup
XM_011531126.1:c.1648-297_1648-290dup	XP_011529428.1:n.1648-297_1648-290dup
NM_000132.4:c.1753-297_1753-290dup MANE Select	NP_000123.1:n.1753-297_1753-290dup