Canonical Allele Identifier: CA2466825984

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896046_154896047delinsAG , CM000685.2:g.154896046_154896047delinsAG	GRCh38
NC_000023.10:g.154124321_154124322delinsAG , CM000685.1:g.154124321_154124322delinsAG	GRCh37
NC_000023.9:g.153777515_153777516delinsAG	NCBI36
NG_011403.1:g.131677_131678delinsCT
NG_011403.2:g.131677_131678delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6429+30_6429+31delinsCT MANE Select	ENSP00000353393.4:n.6429+30_6429+31delinsCT
ENST00000360256.8:c.6429+30_6429+31delinsCT	ENSP00000353393.4:n.6429+30_6429+31delinsCT
NM_000132.3:c.6429+30_6429+31delinsCT	NP_000123.1:n.6429+30_6429+31delinsCT
XM_011531126.1:c.6324+30_6324+31delinsCT	XP_011529428.1:n.6324+30_6324+31delinsCT
NM_000132.4:c.6429+30_6429+31delinsCT MANE Select	NP_000123.1:n.6429+30_6429+31delinsCT