Canonical Allele Identifier: CA2695237883
Gene: F8 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928605del , CM000685.2:g.154928605del GRCh38
NC_000023.10:g.154156880del , CM000685.1:g.154156880del GRCh37
NC_000023.9:g.153810074del NCBI36
NG_011403.1:g.99121del
NG_011403.2:g.99121del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5187del MANE Select ENSP00000353393.4:p.Met1730Ter
ENST00000360256.8:c.5187del ENSP00000353393.4:p.Met1730Ter
NM_000132.3:c.5187del NP_000123.1:p.Met1730Ter
XM_011531126.1:c.5082del XP_011529428.1:p.Met1695Ter
NM_000132.4:c.5187del MANE Select NP_000123.1:p.Met1730Ter
Search 100 bp 5'
Search 100 bp 3'