Canonical Allele Identifier: CA2466842800

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154948663_154948664delinsAC , CM000685.2:g.154948663_154948664delinsAC	GRCh38
NC_000023.10:g.154176938_154176939delinsAC , CM000685.1:g.154176938_154176939delinsAC	GRCh37
NC_000023.9:g.153830132_153830133delinsAC	NCBI36
NG_011403.1:g.79060_79061delinsGT
NG_011403.2:g.79060_79061delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1904-757_1904-756delinsGT MANE Select	ENSP00000353393.4:n.1904-757_1904-756delinsGT
ENST00000647125.1:c.*1779+5228_*1779+5229delinsGT	ENSP00000496062.1:n.*1779+5228_*1779+5229delinsGT
ENST00000360256.8:c.1904-757_1904-756delinsGT	ENSP00000353393.4:n.1904-757_1904-756delinsGT
NM_000132.3:c.1904-757_1904-756delinsGT	NP_000123.1:n.1904-757_1904-756delinsGT
XM_011531126.1:c.1799-757_1799-756delinsGT	XP_011529428.1:n.1799-757_1799-756delinsGT
NM_000132.4:c.1904-757_1904-756delinsGT MANE Select	NP_000123.1:n.1904-757_1904-756delinsGT