Canonical Allele Identifier: CA2466827605
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154902019_154902021delinsGGT , CM000685.2:g.154902019_154902021delinsGGT GRCh38
NC_000023.10:g.154130294_154130296delinsGGT , CM000685.1:g.154130294_154130296delinsGGT GRCh37
NC_000023.9:g.153783488_153783490delinsGGT NCBI36
NG_011403.1:g.125703_125705delinsACC
NG_011403.2:g.125703_125705delinsACC

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6115+30_6115+32delinsACC MANE Select ENSP00000353393.4:n.6115+30_6115+32delins...
ENST00000360256.8:c.6115+30_6115+32delinsACC ENSP00000353393.4:n.6115+30_6115+32delins...
NM_000132.3:c.6115+30_6115+32delinsACC NP_000123.1:n.6115+30_6115+32delinsACC
XM_011531126.1:c.6010+30_6010+32delinsACC XP_011529428.1:n.6010+30_6010+32delinsACC...
NM_000132.4:c.6115+30_6115+32delinsACC MANE Select NP_000123.1:n.6115+30_6115+32delinsACC