Canonical Allele Identifier: CA2695238534
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022464dup , CM000685.2:g.155022464dup GRCh38
NC_000023.10:g.154250739dup , CM000685.1:g.154250739dup GRCh37
NC_000023.9:g.153903933dup NCBI36
NG_011403.1:g.5261dup
NG_011403.2:g.5261dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.90dup MANE Select ENSP00000353393.4:p.Leu31ThrfsTer9
ENST00000647125.1:c.90dup ENSP00000496062.1:p.Leu31ThrfsTer9
ENST00000360256.8:c.90dup ENSP00000353393.4:p.Leu31ThrfsTer9
ENST00000423959.5:c.38+4317dup ENSP00000409446.1:n.38+4317dup
ENST00000453950.1:c.72dup ENSP00000389153.1:p.Leu25ThrfsTer9
NM_000132.3:c.90dup NP_000123.1:p.Leu31ThrfsTer9
XM_011531126.1:c.38+4317dup XP_011529428.1:n.38+4317dup
NM_000132.4:c.90dup MANE Select NP_000123.1:p.Leu31ThrfsTer9
Search 100 bp 5'
Search 100 bp 3'