Canonical Allele Identifier: CA2824314870

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904633_154904634insCACACCC , CM000685.2:g.154904633_154904634insCACACCC	GRCh38
NC_000023.10:g.154132908_154132909insCACACCC , CM000685.1:g.154132908_154132909insCACACCC	GRCh37
NC_000023.9:g.153786102_153786103insCACACCC	NCBI36
NG_011403.1:g.123090_123091insGGGTGTG
NG_011403.2:g.123090_123091insGGGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5587-110_5587-109insGGGTGTG MANE Select	ENSP00000353393.4:n.5587-110_5587-109insGGGTGTG
ENST00000360256.8:c.5587-110_5587-109insGGGTGTG	ENSP00000353393.4:n.5587-110_5587-109insGGGTGTG
NM_000132.3:c.5587-110_5587-109insGGGTGTG	NP_000123.1:n.5587-110_5587-109insGGGTGTG
XM_011531126.1:c.5482-110_5482-109insGGGTGTG	XP_011529428.1:n.5482-110_5482-109insGGGTGTG
NM_000132.4:c.5587-110_5587-109insGGGTGTG MANE Select	NP_000123.1:n.5587-110_5587-109insGGGTGTG