Canonical Allele Identifier: CA13473547
Gene: FEZ1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.125454069C>T , CM000673.2:g.125454069C>T GRCh38
NC_000011.9:g.125323965C>T , CM000673.1:g.125323965C>T GRCh37
NC_000011.8:g.124829175C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000278919.8:c.1020+61G>A MANE Select ENSP00000278919.3:n.1020+61G>A
ENST00000648911.1:c.1020+61G>A ENSP00000497070.1:n.1020+61G>A
ENST00000278919.7:c.1020+61G>A ENSP00000278919.3:n.1020+61G>A
ENST00000524427.5:n.533+61G>A
ENST00000527350.5:n.417+61G>A
ENST00000528863.5:n.228+61G>A
NM_005103.4:c.1020+61G>A NP_005094.1:n.1020+61G>A
XM_005271734.2:c.1020+61G>A XP_005271791.1:n.1020+61G>A
XM_005271735.2:c.1020+61G>A XP_005271792.1:n.1020+61G>A
NM_005103.5:c.1020+61G>A MANE Select NP_005094.1:n.1020+61G>A
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