Canonical Allele Identifier: CA915940900
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154957152del , CM000685.2:g.154957152del GRCh38
NC_000023.10:g.154185427del , CM000685.1:g.154185427del GRCh37
NC_000023.9:g.153838621del NCBI36
NG_011403.1:g.70575del
NG_011403.2:g.70575del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1560del MANE Select ENSP00000353393.4:p.Pro521GlnfsTer14
ENST00000647125.1:c.*1436del ENSP00000496062.1:n.*1436del
ENST00000360256.8:c.1560del ENSP00000353393.4:p.Pro521GlnfsTer14
NM_000132.3:c.1560del NP_000123.1:p.Pro521GlnfsTer14
XM_011531126.1:c.1455del XP_011529428.1:p.Pro486GlnfsTer14
NM_000132.4:c.1560del MANE Select NP_000123.1:p.Pro521GlnfsTer14
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