Canonical Allele Identifier: CA2466844314
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154953900_154953901delinsAT , CM000685.2:g.154953900_154953901delinsAT GRCh38
NC_000023.10:g.154182175_154182176delinsAT , CM000685.1:g.154182175_154182176delinsAT GRCh37
NC_000023.9:g.153835369_153835370delinsAT NCBI36
NG_011403.1:g.73823_73824delinsAT
NG_011403.2:g.73823_73824delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1894_1895delinsAT MANE Select ENSP00000353393.4:p.Ile632=
ENST00000647125.1:c.*1770_*1771delinsAT ENSP00000496062.1:n.*1770_*1771delinsAT
ENST00000360256.8:c.1894_1895delinsAT ENSP00000353393.4:p.Ile632=
NM_000132.3:c.1894_1895delinsAT NP_000123.1:p.Ile632=
XM_011531126.1:c.1789_1790delinsAT XP_011529428.1:p.Ile597=
NM_000132.4:c.1894_1895delinsAT MANE Select NP_000123.1:p.Ile632=
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