Canonical Allele Identifier: CA645238387

Gene: F8

Linked Data

• dbSNP Id: rs1557272769
• gnomAD v2: X-154088672-TC-T
• gnomAD v4: X-154860397-TC-T
• MyVariant Identifiers: chrX:g.154088673del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860398del , CM000685.2:g.154860398del	GRCh38
NC_000023.10:g.154088673del , CM000685.1:g.154088673del	GRCh37
NC_000023.9:g.153741867del	NCBI36
NG_011403.1:g.167326del
NG_011403.2:g.167326del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6900+34del MANE Select	ENSP00000353393.4:n.6900+34del
ENST00000644698.1:c.633+34del	ENSP00000495706.1:n.633+34del
ENST00000330287.10:c.495+34del	ENSP00000327895.6:n.495+34del
ENST00000360256.8:c.6900+34del	ENSP00000353393.4:n.6900+34del
NM_000132.3:c.6900+34del	NP_000123.1:n.6900+34del
NM_019863.2:c.495+34del	NP_063916.1:n.495+34del
XM_011531126.1:c.6795+34del	XP_011529428.1:n.6795+34del
NM_000132.4:c.6900+34del MANE Select	NP_000123.1:n.6900+34del
NM_019863.3:c.495+34del	NP_063916.1:n.495+34del