Canonical Allele Identifier: CA2579753319

Gene: F8

Linked Data

• gnomAD v4: X-155022325-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022327del , CM000685.2:g.155022327del	GRCh38
NC_000023.10:g.154250602del , CM000685.1:g.154250602del	GRCh37
NC_000023.9:g.153903796del	NCBI36
NG_011403.1:g.5398del
NG_011403.2:g.5398del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.143+84del MANE Select	ENSP00000353393.4:n.143+84del
ENST00000647125.1:c.121+106del	ENSP00000496062.1:n.121+106del
ENST00000360256.8:c.143+84del	ENSP00000353393.4:n.143+84del
ENST00000423959.5:c.38+4454del	ENSP00000409446.1:n.38+4454del
ENST00000453950.1:c.125+84del	ENSP00000389153.1:n.125+84del
NM_000132.3:c.143+84del	NP_000123.1:n.143+84del
XM_011531126.1:c.38+4454del	XP_011529428.1:n.38+4454del
NM_000132.4:c.143+84del MANE Select	NP_000123.1:n.143+84del