Canonical Allele Identifier: CA2466828146
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903949_154903950delinsTC , CM000685.2:g.154903949_154903950delinsTC GRCh38
NC_000023.10:g.154132224_154132225delinsTC , CM000685.1:g.154132224_154132225delinsTC GRCh37
NC_000023.9:g.153785418_153785419delinsTC NCBI36
NG_011403.1:g.123774_123775delinsGA
NG_011403.2:g.123774_123775delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5954_5955delinsGA MANE Select ENSP00000353393.4:p.Arg1985=
ENST00000360256.8:c.5954_5955delinsGA ENSP00000353393.4:p.Arg1985=
NM_000132.3:c.5954_5955delinsGA NP_000123.1:p.Arg1985=
XM_011531126.1:c.5849_5850delinsGA XP_011529428.1:p.Arg1950=
NM_000132.4:c.5954_5955delinsGA MANE Select NP_000123.1:p.Arg1985=