Canonical Allele Identifier: CA873360743

Gene: F8

Linked Data

• dbSNP Id: rs1210974402
• gnomAD v3: X-154837579-G-GTGC
• gnomAD v4: X-154837579-G-GTGC
• MyVariant Identifiers: chrX:g.154837579_154837580insTGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837583_154837585dup , CM000685.2:g.154837583_154837585dup	GRCh38
NC_000023.10:g.154065858_154065860dup , CM000685.1:g.154065858_154065860dup	GRCh37
NC_000023.9:g.153719052_153719054dup	NCBI36
NG_011403.1:g.190142_190144dup
NG_033065.1:g.2081_2083dup
NG_011403.2:g.190142_190144dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.*15_*17dup MANE Select	ENSP00000353393.4:n.*15_*17dup
ENST00000644698.1:c.*15_*17dup	ENSP00000495706.1:n.*15_*17dup
ENST00000330287.10:c.*15_*17dup	ENSP00000327895.6:n.*15_*17dup
ENST00000360256.8:c.*15_*17dup	ENSP00000353393.4:n.*15_*17dup
NM_000132.3:c.*15_*17dup	NP_000123.1:n.*15_*17dup
NM_019863.2:c.*15_*17dup	NP_063916.1:n.*15_*17dup
XM_011531126.1:c.*15_*17dup	XP_011529428.1:n.*15_*17dup
NM_000132.4:c.*15_*17dup MANE Select	NP_000123.1:n.*15_*17dup
NM_019863.3:c.*15_*17dup	NP_063916.1:n.*15_*17dup