Canonical Allele Identifier: CA2695238541
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022480dup , CM000685.2:g.155022480dup GRCh38
NC_000023.10:g.154250755dup , CM000685.1:g.154250755dup GRCh37
NC_000023.9:g.153903949dup NCBI36
NG_011403.1:g.5244dup
NG_011403.2:g.5244dup

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.73dup MANE Select ENSP00000353393.4:p.Tyr25LeufsTer15
ENST00000647125.1:c.73dup ENSP00000496062.1:p.Tyr25LeufsTer15
ENST00000360256.8:c.73dup ENSP00000353393.4:p.Tyr25LeufsTer15
ENST00000423959.5:c.38+4300dup ENSP00000409446.1:n.38+4300dup
ENST00000453950.1:c.55dup ENSP00000389153.1:p.Tyr19LeufsTer15
NM_000132.3:c.73dup NP_000123.1:p.Tyr25LeufsTer15
XM_011531126.1:c.38+4300dup XP_011529428.1:n.38+4300dup
NM_000132.4:c.73dup MANE Select NP_000123.1:p.Tyr25LeufsTer15
Search 100 bp 5'
Search 100 bp 3'