Canonical Allele Identifier: CA2824314867

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904615_154904616insACA , CM000685.2:g.154904615_154904616insACA	GRCh38
NC_000023.10:g.154132890_154132891insACA , CM000685.1:g.154132890_154132891insACA	GRCh37
NC_000023.9:g.153786084_153786085insACA	NCBI36
NG_011403.1:g.123108_123109insTGT
NG_011403.2:g.123108_123109insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5587-92_5587-91insTGT MANE Select	ENSP00000353393.4:n.5587-92_5587-91insTGT
ENST00000360256.8:c.5587-92_5587-91insTGT	ENSP00000353393.4:n.5587-92_5587-91insTGT
NM_000132.3:c.5587-92_5587-91insTGT	NP_000123.1:n.5587-92_5587-91insTGT
XM_011531126.1:c.5482-92_5482-91insTGT	XP_011529428.1:n.5482-92_5482-91insTGT
NM_000132.4:c.5587-92_5587-91insTGT MANE Select	NP_000123.1:n.5587-92_5587-91insTGT