Canonical Allele Identifier: CA2695170427

Gene: F8

Linked Data

• gnomAD v4: X-155022293-T-TGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022293_155022294insGGG , CM000685.2:g.155022293_155022294insGGG	GRCh38
NC_000023.10:g.154250568_154250569insGGG , CM000685.1:g.154250568_154250569insGGG	GRCh37
NC_000023.9:g.153903762_153903763insGGG	NCBI36
NG_011403.1:g.5430_5431insCCC
NG_011403.2:g.5430_5431insCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.143+116_143+117insCCC MANE Select	ENSP00000353393.4:n.143+116_143+117insCCC
ENST00000647125.1:c.121+138_121+139insCCC	ENSP00000496062.1:n.121+138_121+139insCCC
ENST00000360256.8:c.143+116_143+117insCCC	ENSP00000353393.4:n.143+116_143+117insCCC
ENST00000423959.5:c.38+4486_38+4487insCCC	ENSP00000409446.1:n.38+4486_38+4487insCCC
ENST00000453950.1:c.125+116_125+117insCCC	ENSP00000389153.1:n.125+116_125+117insCCC
NM_000132.3:c.143+116_143+117insCCC	NP_000123.1:n.143+116_143+117insCCC
XM_011531126.1:c.38+4486_38+4487insCCC	XP_011529428.1:n.38+4486_38+4487insCCC
NM_000132.4:c.143+116_143+117insCCC MANE Select	NP_000123.1:n.143+116_143+117insCCC