Canonical Allele Identifier: CA2824314861

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904156_154904157insCACACCC , CM000685.2:g.154904156_154904157insCACACCC	GRCh38
NC_000023.10:g.154132431_154132432insCACACCC , CM000685.1:g.154132431_154132432insCACACCC	GRCh37
NC_000023.9:g.153785625_153785626insCACACCC	NCBI36
NG_011403.1:g.123567_123568insGGGTGTG
NG_011403.2:g.123567_123568insGGGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5816-69_5816-68insGGGTGTG MANE Select	ENSP00000353393.4:n.5816-69_5816-68insGGGTGTG
ENST00000360256.8:c.5816-69_5816-68insGGGTGTG	ENSP00000353393.4:n.5816-69_5816-68insGGGTGTG
NM_000132.3:c.5816-69_5816-68insGGGTGTG	NP_000123.1:n.5816-69_5816-68insGGGTGTG
XM_011531126.1:c.5711-69_5711-68insGGGTGTG	XP_011529428.1:n.5711-69_5711-68insGGGTGTG
NM_000132.4:c.5816-69_5816-68insGGGTGTG MANE Select	NP_000123.1:n.5816-69_5816-68insGGGTGTG