Canonical Allele Identifier: CA645292862

Gene: F8

Linked Data

• dbSNP Id: rs1438671882
• gnomAD v2: X-154185144-CTA-C
• gnomAD v4: X-154956869-CTA-C
• MyVariant Identifiers: chrX:g.154185145_154185146del (hg19) ; chrX:g.154956870_154956871del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154956873_154956874del , CM000685.2:g.154956873_154956874del	GRCh38
NC_000023.10:g.154185148_154185149del , CM000685.1:g.154185148_154185149del	GRCh37
NC_000023.9:g.153838342_153838343del	NCBI36
NG_011403.1:g.70853_70854del
NG_011403.2:g.70853_70854del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.1752+86_1752+87del MANE Select	ENSP00000353393.4:n.1752+86_1752+87del
ENST00000647125.1:c.*1628+86_*1628+87del	ENSP00000496062.1:n.*1628+86_*1628+87del
ENST00000360256.8:c.1752+86_1752+87del	ENSP00000353393.4:n.1752+86_1752+87del
NM_000132.3:c.1752+86_1752+87del	NP_000123.1:n.1752+86_1752+87del
XM_011531126.1:c.1647+86_1647+87del	XP_011529428.1:n.1647+86_1647+87del
NM_000132.4:c.1752+86_1752+87del MANE Select	NP_000123.1:n.1752+86_1752+87del