Canonical Allele Identifier: CA390175062
Community Standard Title: NM_015346.4(ZFYVE26):c.2149G>T (p.Gly717Ter)
Gene: ZFYVE26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67798113C>A , CM000676.2:g.67798113C>A GRCh38
NC_000014.8:g.68264830C>A , CM000676.1:g.68264830C>A GRCh37
NC_000014.7:g.67334583C>A NCBI36
NG_011836.1:g.23477G>T

Transcript Alleles

HGVS Amino-acid Change
NM_015346.4:c.2149G>T MANE Select NP_056161.2:p.Gly717Ter
ENST00000347230.9:c.2149G>T MANE Select ENSP00000251119.5:p.Gly717Ter
NM_015346.3:c.2149G>T NP_056161.2:p.Gly717Ter
ENST00000347230.8:c.2149G>T ENSP00000251119.5:p.Gly717Ter
ENST00000554523.5:n.2286G>T
ENST00000554557.5:c.*446G>T ENSP00000450431.1:n.*446G>T
ENST00000555452.1:c.2149G>T ENSP00000450603.1:p.Gly717Ter
ENST00000557366.5:n.2195G>T
ENST00000557407.1:n.2284G>T
ENST00000676512.1:c.2149G>T ENSP00000504552.1:p.Gly717Ter
ENST00000676620.1:c.2149G>T ENSP00000504587.1:p.Gly717Ter
ENST00000677026.1:c.1945G>T ENSP00000503710.1:p.Gly649Ter
ENST00000678382.1:c.*1144G>T ENSP00000504130.1:n.*1144G>T
ENST00000678386.1:c.2149G>T ENSP00000503677.1:p.Gly717Ter
XM_006720093.2:c.2149G>T XP_006720156.1:p.Gly717Ter
XM_011536606.1:c.640G>T XP_011534908.1:p.Gly214Ter
XM_011536609.1:c.2149G>T XP_011534911.1:p.Gly717Ter
XM_011536609.2:c.2149G>T XP_011534911.1:p.Gly717Ter
XM_017021124.1:c.2149G>T XP_016876613.1:p.Gly717Ter
XM_017021125.1:c.2149G>T XP_016876614.1:p.Gly717Ter
XM_017021126.1:c.640G>T XP_016876615.1:p.Gly214Ter