Canonical Allele Identifier: CA2695170421

Gene: F8

Linked Data

• gnomAD v4: X-155022282-CCAGAAATGTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022283_155022292del , CM000685.2:g.155022283_155022292del	GRCh38
NC_000023.10:g.154250558_154250567del , CM000685.1:g.154250558_154250567del	GRCh37
NC_000023.9:g.153903752_153903761del	NCBI36
NG_011403.1:g.5432_5441del
NG_011403.2:g.5432_5441del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.143+118_143+127del MANE Select	ENSP00000353393.4:n.143+118_143+127del
ENST00000647125.1:c.121+140_121+149del	ENSP00000496062.1:n.121+140_121+149del
ENST00000360256.8:c.143+118_143+127del	ENSP00000353393.4:n.143+118_143+127del
ENST00000423959.5:c.38+4488_38+4497del	ENSP00000409446.1:n.38+4488_38+4497del
ENST00000453950.1:c.125+118_125+127del	ENSP00000389153.1:n.125+118_125+127del
NM_000132.3:c.143+118_143+127del	NP_000123.1:n.143+118_143+127del
XM_011531126.1:c.38+4488_38+4497del	XP_011529428.1:n.38+4488_38+4497del
NM_000132.4:c.143+118_143+127del MANE Select	NP_000123.1:n.143+118_143+127del