Canonical Allele Identifier: CA2523209906
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154954078_154954082del , CM000685.2:g.154954078_154954082del GRCh38
NC_000023.10:g.154182353_154182357del , CM000685.1:g.154182353_154182357del GRCh37
NC_000023.9:g.153835547_153835551del NCBI36
NG_011403.1:g.73642_73646del
NG_011403.2:g.73642_73646del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1753-40_1753-36del MANE Select ENSP00000353393.4:n.1753-40_1753-36del
ENST00000647125.1:c.*1629-40_*1629-36del ENSP00000496062.1:n.*1629-40_*1629-36del
ENST00000360256.8:c.1753-40_1753-36del ENSP00000353393.4:n.1753-40_1753-36del
NM_000132.3:c.1753-40_1753-36del NP_000123.1:n.1753-40_1753-36del
XM_011531126.1:c.1648-40_1648-36del XP_011529428.1:n.1648-40_1648-36del
NM_000132.4:c.1753-40_1753-36del MANE Select NP_000123.1:n.1753-40_1753-36del