Canonical Allele Identifier: CA2824314886

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154905049_154905050insCCCC , CM000685.2:g.154905049_154905050insCCCC	GRCh38
NC_000023.10:g.154133324_154133325insCCCC , CM000685.1:g.154133324_154133325insCCCC	GRCh37
NC_000023.9:g.153786518_153786519insCCCC	NCBI36
NG_011403.1:g.122674_122675insGGGG
NG_011403.2:g.122674_122675insGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5374-27_5374-26insGGGG MANE Select	ENSP00000353393.4:n.5374-27_5374-26insGGGG
ENST00000360256.8:c.5374-27_5374-26insGGGG	ENSP00000353393.4:n.5374-27_5374-26insGGGG
NM_000132.3:c.5374-27_5374-26insGGGG	NP_000123.1:n.5374-27_5374-26insGGGG
XM_011531126.1:c.5269-27_5269-26insGGGG	XP_011529428.1:n.5269-27_5269-26insGGGG
NM_000132.4:c.5374-27_5374-26insGGGG MANE Select	NP_000123.1:n.5374-27_5374-26insGGGG