Canonical Allele Identifier: CA2466865426

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022465_155022470delinsCCACTG , CM000685.2:g.155022465_155022470delinsCCACTG	GRCh38
NC_000023.10:g.154250740_154250745delinsCCACTG , CM000685.1:g.154250740_154250745delinsCCACTG	GRCh37
NC_000023.9:g.153903934_153903939delinsCCACTG	NCBI36
NG_011403.1:g.5254_5259delinsCAGTGG
NG_011403.2:g.5254_5259delinsCAGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.83_88delinsCAGTGG MANE Select	ENSP00000353393.4:p.Ala28=
ENST00000647125.1:c.83_88delinsCAGTGG	ENSP00000496062.1:p.Ala28=
ENST00000360256.8:c.83_88delinsCAGTGG	ENSP00000353393.4:p.Ala28=
ENST00000423959.5:c.38+4310_38+4315delinsCAGTGG	ENSP00000409446.1:n.38+4310_38+4315delinsCAGTGG
ENST00000453950.1:c.65_70delinsCAGTGG	ENSP00000389153.1:p.Ala22=
NM_000132.3:c.83_88delinsCAGTGG	NP_000123.1:p.Ala28=
XM_011531126.1:c.38+4310_38+4315delinsCAGTGG	XP_011529428.1:n.38+4310_38+4315delinsCAGTGG
NM_000132.4:c.83_88delinsCAGTGG MANE Select	NP_000123.1:p.Ala28=