Canonical Allele Identifier: CA2824314871

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904634_154904635insCACACCCAAC , CM000685.2:g.154904634_154904635insCACACCCAAC	GRCh38
NC_000023.10:g.154132909_154132910insCACACCCAAC , CM000685.1:g.154132909_154132910insCACACCCAAC	GRCh37
NC_000023.9:g.153786103_153786104insCACACCCAAC	NCBI36
NG_011403.1:g.123089_123090insGTTGGGTGTG
NG_011403.2:g.123089_123090insGTTGGGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5587-111_5587-110insGTTGGGTGTG MANE Select	ENSP00000353393.4:n.5587-111_5587-110insGTTGGGTGTG
ENST00000360256.8:c.5587-111_5587-110insGTTGGGTGTG	ENSP00000353393.4:n.5587-111_5587-110insGTTGGGTGTG
NM_000132.3:c.5587-111_5587-110insGTTGGGTGTG	NP_000123.1:n.5587-111_5587-110insGTTGGGTGTG
XM_011531126.1:c.5482-111_5482-110insGTTGGGTGTG	XP_011529428.1:n.5482-111_5482-110insGTTGGGTGTG
NM_000132.4:c.5587-111_5587-110insGTTGGGTGTG MANE Select	NP_000123.1:n.5587-111_5587-110insGTTGGGTGTG