Canonical Allele Identifier: CA7239845
Community Standard Title: NM_015346.4(ZFYVE26):c.4061G>A (p.Arg1354Gln)
Gene: ZFYVE26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67783091C>T , CM000676.2:g.67783091C>T GRCh38
NC_000014.8:g.68249808C>T , CM000676.1:g.68249808C>T GRCh37
NC_000014.7:g.67319561C>T NCBI36
NG_011836.1:g.38499G>A

Transcript Alleles

HGVS Amino-acid Change
NM_015346.4:c.4061G>A MANE Select NP_056161.2:p.Arg1354Gln
ENST00000347230.9:c.4061G>A MANE Select ENSP00000251119.5:p.Arg1354Gln
NM_015346.3:c.4061G>A NP_056161.2:p.Arg1354Gln
ENST00000347230.8:c.4061G>A ENSP00000251119.5:p.Arg1354Gln
ENST00000554523.5:n.4198G>A
ENST00000554557.5:c.*2350+8G>A ENSP00000450431.1:n.*2350+8G>A
ENST00000555452.1:c.4061G>A ENSP00000450603.1:p.Arg1354Gln
ENST00000676512.1:c.4061G>A ENSP00000504552.1:p.Arg1354Gln
ENST00000676620.1:c.4061G>A ENSP00000504587.1:p.Arg1354Gln
ENST00000678386.1:c.4061G>A ENSP00000503677.1:p.Arg1354Gln
XM_006720093.2:c.4061G>A XP_006720156.1:p.Arg1354Gln
XM_011536606.1:c.2552G>A XP_011534908.1:p.Arg851Gln
XM_011536607.1:c.1736G>A XP_011534909.1:p.Arg579Gln
XM_011536608.1:c.1643G>A XP_011534910.1:p.Arg548Gln
XM_011536609.1:c.4061G>A XP_011534911.1:p.Arg1354Gln
XM_011536609.2:c.4061G>A XP_011534911.1:p.Arg1354Gln
XM_017021124.1:c.4061G>A XP_016876613.1:p.Arg1354Gln
XM_017021125.1:c.4061G>A XP_016876614.1:p.Arg1354Gln
XM_017021126.1:c.2552G>A XP_016876615.1:p.Arg851Gln
XM_017021127.2:c.1736G>A XP_016876616.1:p.Arg579Gln
XM_017021128.1:c.1643G>A XP_016876617.1:p.Arg548Gln