Canonical Allele Identifier: CA390176554
Community Standard Title: NM_015346.4(ZFYVE26):c.1477C>A (p.Gln493Lys)
Gene: ZFYVE26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67802241G>T , CM000676.2:g.67802241G>T GRCh38
NC_000014.8:g.68268958G>T , CM000676.1:g.68268958G>T GRCh37
NC_000014.7:g.67338711G>T NCBI36
NG_011836.1:g.19349C>A

Transcript Alleles

HGVS Amino-acid Change
NM_015346.4:c.1477C>A MANE Select NP_056161.2:p.Gln493Lys
ENST00000347230.9:c.1477C>A MANE Select ENSP00000251119.5:p.Gln493Lys
NM_015346.3:c.1477C>A NP_056161.2:p.Gln493Lys
ENST00000347230.8:c.1477C>A ENSP00000251119.5:p.Gln493Lys
ENST00000554523.5:n.1614C>A
ENST00000554557.5:c.1271+2976C>A ENSP00000450431.1:n.1271+2976C>A
ENST00000555452.1:c.1477C>A ENSP00000450603.1:p.Gln493Lys
ENST00000557366.5:n.1523C>A
ENST00000557407.1:n.1612C>A
ENST00000676512.1:c.1477C>A ENSP00000504552.1:p.Gln493Lys
ENST00000676620.1:c.1477C>A ENSP00000504587.1:p.Gln493Lys
ENST00000677026.1:c.1435+1860C>A ENSP00000503710.1:n.1435+1860C>A
ENST00000678382.1:c.*472C>A ENSP00000504130.1:n.*472C>A
ENST00000678386.1:c.1477C>A ENSP00000503677.1:p.Gln493Lys
XM_006720093.2:c.1477C>A XP_006720156.1:p.Gln493Lys
XM_011536606.1:c.-33C>A XP_011534908.1:n.-33C>A
XM_011536609.1:c.1477C>A XP_011534911.1:p.Gln493Lys
XM_011536609.2:c.1477C>A XP_011534911.1:p.Gln493Lys
XM_017021124.1:c.1477C>A XP_016876613.1:p.Gln493Lys
XM_017021125.1:c.1477C>A XP_016876614.1:p.Gln493Lys
XM_017021126.1:c.-33C>A XP_016876615.1:n.-33C>A