Canonical Allele Identifier: CA2573055171
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1331083
ClinVar RCV Id: RCV001802742
dbSNP Id: rs2148555575

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837679del , CM000685.2:g.154837679del GRCh38
NC_000023.10:g.154065954del , CM000685.1:g.154065954del GRCh37
NC_000023.9:g.153719148del NCBI36
NG_011403.1:g.190046del
NG_033065.1:g.1985del
NG_011403.2:g.190046del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6975del MANE Select ENSP00000353393.4:p.Arg2326GlufsTer13
ENST00000644698.1:c.708del ENSP00000495706.1:p.Arg237GlufsTer13
ENST00000330287.10:c.570del ENSP00000327895.6:p.Arg191GlufsTer13
ENST00000360256.8:c.6975del ENSP00000353393.4:p.Arg2326GlufsTer13
NM_000132.3:c.6975del NP_000123.1:p.Arg2326GlufsTer13
NM_019863.2:c.570del NP_063916.1:p.Arg191GlufsTer13
XM_011531126.1:c.6870del XP_011529428.1:p.Arg2291GlufsTer13
NM_000132.4:c.6975del MANE Select NP_000123.1:p.Arg2326GlufsTer13
NM_019863.3:c.570del NP_063916.1:p.Arg191GlufsTer13