Canonical Allele Identifier: CA1571013789
Gene: FBXL17 HGNC NCBI

Linked Data

dbSNP Id: rs1751261102
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.107945776G>C , CM000667.2:g.107945776G>C GRCh38
NC_000005.9:g.107281477G>C , CM000667.1:g.107281477G>C GRCh37
NC_000005.8:g.107309376G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000496714.2:c.831-64597C>G
ENST00000542267.7:c.1823-64597C>G MANE Select ENSP00000437464.2:n.1823-64597C>G
ENST00000359660.9:c.629-64597C>G ENSP00000352683.4:n.629-64597C>G
ENST00000496714.1:c.629-64597C>G ENSP00000418111.1:n.629-64597C>G
ENST00000542267.5:c.1823-64597C>G ENSP00000437464.1:n.1823-64597C>G
ENST00000619412.4:c.1109-64597C>G ENSP00000481439.1:n.1109-64597C>G
NM_001163315.2:c.1823-64597C>G NP_001156787.2:n.1823-64597C>G
XM_005272048.3:c.1823-64597C>G XP_005272105.1:n.1823-64597C>G
XM_005272048.4:c.1823-64597C>G XP_005272105.1:n.1823-64597C>G
NM_001163315.3:c.1823-64597C>G MANE Select NP_001156787.2:n.1823-64597C>G
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