Canonical Allele Identifier: CA114478
Gene: ZFYVE26 HGNC NCBI

Linked Data

ClinVar Variation Id: 752
ClinVar RCV Id: RCV000000788
dbSNP Id: rs118204050

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000347230.9:c.1477C>T MANE Select ENSP00000251119.5:p.Gln493Ter
ENST00000676512.1:c.1477C>T ENSP00000504552.1:p.Gln493Ter
ENST00000676620.1:c.1477C>T ENSP00000504587.1:p.Gln493Ter
ENST00000677026.1:c.1435+1860C>T ENSP00000503710.1:n.1435+1860C>T
ENST00000678382.1:c.*472C>T ENSP00000504130.1:n.*472C>T
ENST00000678386.1:c.1477C>T ENSP00000503677.1:p.Gln493Ter
ENST00000347230.8:c.1477C>T ENSP00000251119.5:p.Gln493Ter
ENST00000554523.5:n.1614C>T
ENST00000554557.5:c.1271+2976C>T ENSP00000450431.1:n.1271+2976C>T
ENST00000555452.1:c.1477C>T ENSP00000450603.1:p.Gln493Ter
ENST00000557366.5:n.1523C>T
ENST00000557407.1:n.1612C>T
NM_015346.3:c.1477C>T NP_056161.2:p.Gln493Ter
XM_006720093.2:c.1477C>T XP_006720156.1:p.Gln493Ter
XM_011536606.1:c.-33C>T XP_011534908.1:n.-33C>T
XM_011536609.1:c.1477C>T XP_011534911.1:p.Gln493Ter
XM_011536609.2:c.1477C>T XP_011534911.1:p.Gln493Ter
XM_017021124.1:c.1477C>T XP_016876613.1:p.Gln493Ter
XM_017021125.1:c.1477C>T XP_016876614.1:p.Gln493Ter
XM_017021126.1:c.-33C>T XP_016876615.1:n.-33C>T
NM_015346.4:c.1477C>T MANE Select NP_056161.2:p.Gln493Ter