Canonical Allele Identifier: CA2695237202

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154947727_154947728delinsA , CM000685.2:g.154947727_154947728delinsA	GRCh38
NC_000023.10:g.154176002_154176003delinsA , CM000685.1:g.154176002_154176003delinsA	GRCh37
NC_000023.9:g.153829196_153829197delinsA	NCBI36
NG_011403.1:g.79996_79997delinsT
NG_011403.2:g.79996_79997delinsT

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.2083_2084delinsT MANE Select	ENSP00000353393.4:p.Glu695Ter
ENST00000647125.1:c.*1779+6164_*1779+6165delinsT	ENSP00000496062.1:n.*1779+6164_*1779+6165...
ENST00000360256.8:c.2083_2084delinsT	ENSP00000353393.4:p.Glu695Ter
NM_000132.3:c.2083_2084delinsT	NP_000123.1:p.Glu695Ter
XM_011531126.1:c.1978_1979delinsT	XP_011529428.1:p.Glu660Ter
NM_000132.4:c.2083_2084delinsT MANE Select	NP_000123.1:p.Glu695Ter