Canonical Allele Identifier: CA2466828496
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154905040_154905041delinsAC , CM000685.2:g.154905040_154905041delinsAC GRCh38
NC_000023.10:g.154133315_154133316delinsAC , CM000685.1:g.154133315_154133316delinsAC GRCh37
NC_000023.9:g.153786509_153786510delinsAC NCBI36
NG_011403.1:g.122683_122684delinsGT
NG_011403.2:g.122683_122684delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5374-18_5374-17delinsGT MANE Select ENSP00000353393.4:n.5374-18_5374-17delinsGT
ENST00000360256.8:c.5374-18_5374-17delinsGT ENSP00000353393.4:n.5374-18_5374-17delinsGT
NM_000132.3:c.5374-18_5374-17delinsGT NP_000123.1:n.5374-18_5374-17delinsGT
XM_011531126.1:c.5269-18_5269-17delinsGT XP_011529428.1:n.5269-18_5269-17delinsGT
NM_000132.4:c.5374-18_5374-17delinsGT MANE Select NP_000123.1:n.5374-18_5374-17delinsGT