Canonical Allele Identifier: CA2695237934
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903948_154903949del , CM000685.2:g.154903948_154903949del GRCh38
NC_000023.10:g.154132223_154132224del , CM000685.1:g.154132223_154132224del GRCh37
NC_000023.9:g.153785417_153785418del NCBI36
NG_011403.1:g.123780_123781del
NG_011403.2:g.123780_123781del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5960_5961del MANE Select ENSP00000353393.4:p.Lys1987ArgfsTer4
ENST00000360256.8:c.5960_5961del ENSP00000353393.4:p.Lys1987ArgfsTer4
NM_000132.3:c.5960_5961del NP_000123.1:p.Lys1987ArgfsTer4
XM_011531126.1:c.5855_5856del XP_011529428.1:p.Lys1952ArgfsTer4
NM_000132.4:c.5960_5961del MANE Select NP_000123.1:p.Lys1987ArgfsTer4
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