Canonical Allele Identifier: CA7239587
Gene: ZFYVE26 HGNC NCBI

Linked Data

ClinVar Variation Id: 289453
dbSNP Id: rs143981992

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67775960T>G , CM000676.2:g.67775960T>G GRCh38
NC_000014.8:g.68242677T>G , CM000676.1:g.68242677T>G GRCh37
NC_000014.7:g.67312430T>G NCBI36
NG_011836.1:g.45630A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000347230.9:c.5121A>C MANE Select ENSP00000251119.5:p.Gly1707=
ENST00000676512.1:c.5121A>C ENSP00000504552.1:p.Gly1707=
ENST00000676620.1:c.5043A>C ENSP00000504587.1:p.Gly1681=
ENST00000678386.1:c.5166A>C ENSP00000503677.1:p.Gly1722=
ENST00000347230.8:c.5121A>C ENSP00000251119.5:p.Gly1707=
ENST00000554523.5:n.5258A>C
ENST00000554557.5:c.*3099A>C ENSP00000450431.1:n.*3099A>C
ENST00000555452.1:c.5121A>C ENSP00000450603.1:p.Gly1707=
NM_015346.3:c.5121A>C NP_056161.2:p.Gly1707=
XM_006720093.2:c.5121A>C XP_006720156.1:p.Gly1707=
XM_011536606.1:c.3612A>C XP_011534908.1:p.Gly1204=
XM_011536607.1:c.2796A>C XP_011534909.1:p.Gly932=
XM_011536608.1:c.2703A>C XP_011534910.1:p.Gly901=
XM_017021124.1:c.5121A>C XP_016876613.1:p.Gly1707=
XM_017021125.1:c.5121A>C XP_016876614.1:p.Gly1707=
XM_017021126.1:c.3612A>C XP_016876615.1:p.Gly1204=
XM_017021127.2:c.2796A>C XP_016876616.1:p.Gly932=
XM_017021128.1:c.2703A>C XP_016876617.1:p.Gly901=
NM_015346.4:c.5121A>C MANE Select NP_056161.2:p.Gly1707=