Canonical Allele Identifier: CA2533126441

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154948738_154948739insGT , CM000685.2:g.154948738_154948739insGT	GRCh38
NC_000023.10:g.154177013_154177014insGT , CM000685.1:g.154177013_154177014insGT	GRCh37
NC_000023.9:g.153830207_153830208insGT	NCBI36
NG_011403.1:g.78985_78986insAC
NG_011403.2:g.78985_78986insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1904-832_1904-831insAC MANE Select	ENSP00000353393.4:n.1904-832_1904-831insAC
ENST00000647125.1:c.*1779+5153_*1779+5154insAC	ENSP00000496062.1:n.*1779+5153_*1779+5154insAC
ENST00000360256.8:c.1904-832_1904-831insAC	ENSP00000353393.4:n.1904-832_1904-831insAC
NM_000132.3:c.1904-832_1904-831insAC	NP_000123.1:n.1904-832_1904-831insAC
XM_011531126.1:c.1799-832_1799-831insAC	XP_011529428.1:n.1799-832_1799-831insAC
NM_000132.4:c.1904-832_1904-831insAC MANE Select	NP_000123.1:n.1904-832_1904-831insAC