Canonical Allele Identifier: CA10567741

Gene: F8

Linked Data

• dbSNP Id: rs781848666
• ExAC: X:154088669 T / TTTTCTTTC
• MyVariant Identifiers: chrX:g.154088673_154088674insTTTCTTTC (hg19) ; chrX:g.154088669_154088670insTTTCTTTC (hg19) ; chrX:g.154860394_154860395insTTTCTTTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860407_154860414dup , CM000685.2:g.154860407_154860414dup	GRCh38
NC_000023.10:g.154088682_154088689dup , CM000685.1:g.154088682_154088689dup	GRCh37
NC_000023.9:g.153741876_153741883dup	NCBI36
NG_011403.1:g.167322_167329dup
NG_011403.2:g.167322_167329dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6900+30_6900+37dup MANE Select	ENSP00000353393.4:n.6900+30_6900+37dup
ENST00000644698.1:c.633+30_633+37dup	ENSP00000495706.1:n.633+30_633+37dup
ENST00000330287.10:c.495+30_495+37dup	ENSP00000327895.6:n.495+30_495+37dup
ENST00000360256.8:c.6900+30_6900+37dup	ENSP00000353393.4:n.6900+30_6900+37dup
NM_000132.3:c.6900+30_6900+37dup	NP_000123.1:n.6900+30_6900+37dup
NM_019863.2:c.495+30_495+37dup	NP_063916.1:n.495+30_495+37dup
XM_011531126.1:c.6795+30_6795+37dup	XP_011529428.1:n.6795+30_6795+37dup
NM_000132.4:c.6900+30_6900+37dup MANE Select	NP_000123.1:n.6900+30_6900+37dup
NM_019863.3:c.495+30_495+37dup	NP_063916.1:n.495+30_495+37dup