Canonical Allele Identifier: CA2842900044

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022366_155022367del , CM000685.2:g.155022366_155022367del	GRCh38
NC_000023.10:g.154250641_154250642del , CM000685.1:g.154250641_154250642del	GRCh37
NC_000023.9:g.153903835_153903836del	NCBI36
NG_011403.1:g.5359_5360del
NG_011403.2:g.5359_5360del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.143+45_143+46del MANE Select	ENSP00000353393.4:n.143+45_143+46del
ENST00000647125.1:c.121+67_121+68del	ENSP00000496062.1:n.121+67_121+68del
ENST00000360256.8:c.143+45_143+46del	ENSP00000353393.4:n.143+45_143+46del
ENST00000423959.5:c.38+4415_38+4416del	ENSP00000409446.1:n.38+4415_38+4416del
ENST00000453950.1:c.125+45_125+46del	ENSP00000389153.1:n.125+45_125+46del
NM_000132.3:c.143+45_143+46del	NP_000123.1:n.143+45_143+46del
XM_011531126.1:c.38+4415_38+4416del	XP_011529428.1:n.38+4415_38+4416del
NM_000132.4:c.143+45_143+46del MANE Select	NP_000123.1:n.143+45_143+46del