Canonical Allele Identifier: CA920451192

Gene: F8

Linked Data

• dbSNP Id: rs1603437845

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022286_155022292del , CM000685.2:g.155022286_155022292del	GRCh38
NC_000023.10:g.154250561_154250567del , CM000685.1:g.154250561_154250567del	GRCh37
NC_000023.9:g.153903755_153903761del	NCBI36
NG_011403.1:g.5432_5438del
NG_011403.2:g.5432_5438del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.143+118_143+124del MANE Select	ENSP00000353393.4:n.143+118_143+124del
ENST00000647125.1:c.121+140_121+146del	ENSP00000496062.1:n.121+140_121+146del
ENST00000360256.8:c.143+118_143+124del	ENSP00000353393.4:n.143+118_143+124del
ENST00000423959.5:c.38+4488_38+4494del	ENSP00000409446.1:n.38+4488_38+4494del
ENST00000453950.1:c.125+118_125+124del	ENSP00000389153.1:n.125+118_125+124del
NM_000132.3:c.143+118_143+124del	NP_000123.1:n.143+118_143+124del
XM_011531126.1:c.38+4488_38+4494del	XP_011529428.1:n.38+4488_38+4494del
NM_000132.4:c.143+118_143+124del MANE Select	NP_000123.1:n.143+118_143+124del