Canonical Allele Identifier: CA2695237928
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903937_154903940dup , CM000685.2:g.154903937_154903940dup GRCh38
NC_000023.10:g.154132212_154132215dup , CM000685.1:g.154132212_154132215dup GRCh37
NC_000023.9:g.153785406_153785409dup NCBI36
NG_011403.1:g.123784_123787dup
NG_011403.2:g.123784_123787dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5964_5967dup MANE Select ENSP00000353393.4:p.Tyr1990GlyfsTer3
ENST00000360256.8:c.5964_5967dup ENSP00000353393.4:p.Tyr1990GlyfsTer3
NM_000132.3:c.5964_5967dup NP_000123.1:p.Tyr1990GlyfsTer3
XM_011531126.1:c.5859_5862dup XP_011529428.1:p.Tyr1955GlyfsTer3
NM_000132.4:c.5964_5967dup MANE Select NP_000123.1:p.Tyr1990GlyfsTer3
Search 100 bp 5'
Search 100 bp 3'