Canonical Allele Identifier: CA2466828441
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904894_154904895delinsAG , CM000685.2:g.154904894_154904895delinsAG GRCh38
NC_000023.10:g.154133169_154133170delinsAG , CM000685.1:g.154133169_154133170delinsAG GRCh37
NC_000023.9:g.153786363_153786364delinsAG NCBI36
NG_011403.1:g.122829_122830delinsCT
NG_011403.2:g.122829_122830delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5502_5503delinsCT MANE Select ENSP00000353393.4:p.Tyr1834=
ENST00000360256.8:c.5502_5503delinsCT ENSP00000353393.4:p.Tyr1834=
NM_000132.3:c.5502_5503delinsCT NP_000123.1:p.Tyr1834=
XM_011531126.1:c.5397_5398delinsCT XP_011529428.1:p.Tyr1799=
NM_000132.4:c.5502_5503delinsCT MANE Select NP_000123.1:p.Tyr1834=
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