Canonical Allele Identifier: CA2466836679
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154931403_154931404delinsGT , CM000685.2:g.154931403_154931404delinsGT GRCh38
NC_000023.10:g.154159678_154159679delinsGT , CM000685.1:g.154159678_154159679delinsGT GRCh37
NC_000023.9:g.153812872_153812873delinsGT NCBI36
NG_011403.1:g.96320_96321delinsAC
NG_011403.2:g.96320_96321delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.2386_2387delinsAC MANE Select ENSP00000353393.4:p.Thr796=
ENST00000647125.1:c.*2052_*2053delinsAC ENSP00000496062.1:n.*2052_*2053delinsAC
ENST00000360256.8:c.2386_2387delinsAC ENSP00000353393.4:p.Thr796=
NM_000132.3:c.2386_2387delinsAC NP_000123.1:p.Thr796=
XM_011531126.1:c.2281_2282delinsAC XP_011529428.1:p.Thr761=
NM_000132.4:c.2386_2387delinsAC MANE Select NP_000123.1:p.Thr796=
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