Canonical Allele Identifier: CA2824314884

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154905043_154905044insG , CM000685.2:g.154905043_154905044insG	GRCh38
NC_000023.10:g.154133318_154133319insG , CM000685.1:g.154133318_154133319insG	GRCh37
NC_000023.9:g.153786512_153786513insG	NCBI36
NG_011403.1:g.122680_122681insC
NG_011403.2:g.122680_122681insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5374-21_5374-20insC MANE Select	ENSP00000353393.4:n.5374-21_5374-20insC
ENST00000360256.8:c.5374-21_5374-20insC	ENSP00000353393.4:n.5374-21_5374-20insC
NM_000132.3:c.5374-21_5374-20insC	NP_000123.1:n.5374-21_5374-20insC
XM_011531126.1:c.5269-21_5269-20insC	XP_011529428.1:n.5269-21_5269-20insC
NM_000132.4:c.5374-21_5374-20insC MANE Select	NP_000123.1:n.5374-21_5374-20insC